Spindle-shaped magnetic metal particles containing iron as main component and processes for producing the same

ABSTRACT

Spindle-shaped magnetic metal particles containing iron as a main component, having an average major axis diameter (L) of 0.05 to 0.15 μm; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of from 150 to less than 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula: 
     
       
           S ≦−160× L +65; 
       
     
     an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C. The spindle-shaped magnetic metal particles containing iron as a main component, exhibit an adequate coercive force, and are excellent in dispersibility, oxidation stability and coercive force distribution despite fine particles, especially notwithstanding the particles have an average major axis diameter as small as 0.05 to 0.15 μm.

BACKGROUND OF THE INVENTION

The present invention relates to spindle-shaped magnetic metal particles containing iron as a main component and a process for producing the spindle-shaped magnetic metal particles, and more particularly, to spindle-shaped magnetic metal particles containing iron as a main component, which exhibit an adequate coercive force, and are excellent in dispersibility, oxidation stability and coercive force distribution despite fine particles, especially notwithstanding the particles have an average major axis diameter as small as 0.05 to 0.15 μm.

In recent years, recording-time prolongation, miniaturization and lightening of audio, video or computer magnetic recording and reproducing apparatuses for various magnetic recording media such as digital audio tapes (DAT) for people's livelihood use, 8-mm video tapes, Hi-8 tapes, VTR tapes for business use, computer tapes or discs thereof have proceeded more rapidly. In particular, VTRs (video tape recorders) are now widespread, so that there have been intensely developed VTRs aiming at the transfer of analog recording types into digital ones in addition to the above recording-time prolongation, miniaturization and lightening thereof. On the other hand, with such recent tendencies, the magnetic recording media have been required to have high image quality and high output characteristics, especially high frequency characteristics. To meet these requirements, it is necessary to reduce noise due to the magnetic recording media themselves and enhance residual magnetic flux density, coercive force, dispersibility, filling property and tape-surface smoothness thereof. Therefore, it has been further required to improve S/N ratio of the magnetic recording media.

These properties of the magnetic recording media have a close relation to magnetic particles used therein. In recent years, magnetic metal particles containing iron as a main component have been noticed, because such particles can show a higher coercive force and a larger saturation magnetization as compared to those of conventional magnetic iron oxide particles, and such magnetic metal particles containing iron as a main component have been already used as magnetic particles for magnetic recording media such as DAT, 8-mm video tapes, Hi-8 tapes, video tapes for business use, computer tapes or discs. The magnetic metal particles containing iron as a main component conventionally used in DAT, 8-mm video tapes, Hi-8 tapes or the like have been required to be further improved in output characteristics and weather resistance. In addition, the magnetic metal particles containing iron as a main component must fulfill applicability to existing format and good economy at the same time. Therefore, it has been strongly required to provide magnetic metal particles containing iron as a main component capable of satisfying the above requirements while minimizing amounts of various metals added thereto.

Various properties of magnetic recording media are detailed below.

In order to obtain high image quality in video magnetic recording media, it has been required to enhance S/N ratio and video frequency characteristics thereof. For this reason, it is important to improve a surface smoothness of the magnetic recording media. For improving the surface smoothness, it is also required to improve a dispersibility of magnetic particles in coating composition as well as orientation and filling properties thereof in coating film. In addition, in order to enhance the video frequency characteristics, the magnetic recording media have been required to exhibit not only a high coercive force and a large residual magnetic flux density, but also an excellent S.F.D. (Switching Field Distribution), i.e., a small coercive force distribution.

Further, it is important that the magnetic recording media can show good repeat-running property, good still property as well as high recording reliability even when used under severe environmental conditions, i.e., high durability.

As to the magnetic metal particles containing iron as a main component for magnetic recording media capable of satisfying the above various properties, those having a larger particle size are preferable from the standpoint of improvement in dispersibility and oxidation stability. On the contrary, the magnetic metal particles containing iron as a main component, having a smaller particle size are preferable from the standpoint of improvement in surface smoothness and reduction of noise. However, the smaller the particle size of the magnetic metal particles, the poorer the dispersibility and oxidation stability thereof. Also, when the particle size becomes smaller, the coercive force thereof is generally increased. Therefore, it is necessary to appropriately control the particle size for attaining aimed magnetic properties. Further, it is preferable to incorporate a large amount of cobalt into the magnetic metal particles containing iron as a main component in the consideration of chemical composition thereof since as well known in the arts, cobalt forms a solid solution with iron and contributes to improvement in oxidation stability. However, the use of a large amount of expensive cobalt is disadvantageous from economical viewpoint. Consequently, it has been demanded to provide magnetic metal particles containing iron as a main component exhibiting an adequate coercive force as well as excellent dispersibility and oxidation stability despite minimizing contents of expensive metal elements such as cobalt and reducing the particle size.

As known in the arts, the magnetic metal particles containing iron as a main component are produced by heat-treating either goethite particles, hematite particles obtained by heat-dehydrating the goethite particles, or particles obtained by incorporating different metal elements other than iron into the above goethite or hematite particles as starting material, in a non-reducing atmosphere, if required; and then heat-reducing the resultant particles in a reducing atmosphere. In this case, it is required that the obtained magnetic metal particles containing iron as a main component can analogously maintain shape and size of the goethite particles as starting material by appropriately controlling the shape and size of the goethite particles and further by preventing heat fusion between particles upon heat-treatments such as heat-dehydration and heat-reduction, or deformation and shape-breakage of each particle.

The goethite particles as starting material are classified into two kinds of goethite particles according to configurations thereof, i.e., acicular goethite particles produced by using alkali hydroxide, and spindle-shaped goethite particles produced by using alkali carbonate. The acicular goethite particles tend to generally have a large aspect ratio, but tend to be deteriorated in particle size distribution and become large in size as compared to spindle-shaped goethite particles. The particle size distribution is an index of uniformity of primary particles and, therefore, has a close relationship with coercive force distribution and oxidation stability of the magnetic metal particles containing iron as a main component. Consequently, spindle-shaped goethite particles having an excellent particle size distribution are preferably used as the starting materials of the magnetic metal particles containing iron as a main component.

On the other hand, as heat-reducing apparatuses, there are known fluidized a bed-type reducing apparatus for heat-reducing the starting material while fluidizing the material in the form of particles, a fixed-bed-type reducing apparatus for heat-reducing a fixed-bed formed of the starting material which is granulated into granular particles, a moving bed-type reducing apparatus for heat-reducing the starting material while moving the fixed-bed thereof, or the like.

With the increasing demand for developing mass-production techniques in association with the increase in amount of the used magnetic metal particles containing iron as a main component, among the above apparatuses, the fixed-bed-type reducing apparatus (including the moving bed-type reducing apparatus) are preferred from industrial and economical viewpoints, because the apparatus of this type is capable of mass-producing the magnetic metal particles containing iron as a main component without scattering thereof even when a large amount of reducing gas such as hydrogen is flowed therethrough.

However, when the fixed-bed formed from the particles is heat-reduced in a hydrogen atmosphere, a water vapor partial pressure of the reaction system is increased by abrupt reduction caused at a lower portion of the fixed-bed. As a result, the particles located at an upper portion of the fixed-bed tend to suffer from more severe shape breakage or minor axis growth as compared to those located at the lower portion of the fixed-bed, resulting in different properties of the particles obtained from the lower and upper portions of the fixed-bed. Therefore, it becomes difficult to obtain magnetic metal particles containing iron as a main component having uniform properties, as a whole.

In general, it is required that the magnetic metal particles containing iron as a main component can still maintain shape and size of goethite particles or hematite particles as starting material by preventing heat fusion between particles or deformation and shape-breakage of the respective particles. The magnetic metal particles containing iron as a main component suffering from shape-breakage cannot show a high coercive force because of poor shape anisotropy thereof, resulting in deteriorated particle size distribution. Further, upon the production of magnetic recording media, such magnetic metal particles containing iron as a main component show deteriorated dispersibility due to the increase in intermolecular force or magnetic adhesion force between particles when kneaded with a binder resin and dispersed therein. As a result, a magnetic coating film produced from such magnetic metal particles containing iron as a main component is deteriorated in squareness, thereby failing to obtain a magnetic recording medium having an excellent SFD.

Consequently, it has been strongly required to provide a heat-reducing process capable of producing magnetic metal particles containing iron as a main component which are substantially free from shape breakage and can show uniform properties notwithstanding the particles are located at either lower or upper portion of the fixed-bed upon the heat-reduction.

Under these circumstances, as magnetic metal particles containing iron as a main component used for audio or video magnetic recording media such as digital audio tapes (DAT) for general use, 8-mm video tapes and Hi-8 tapes, there have been demanded such magnetic metal particles having an adequate coercive force of 111.4 to 159.2 kA/m (1,400 to 2,000 Oe) as well as good dispersibility and oxidation stability even though the content of expensive elements such as cobalt is minimized and the particle size is reduced in order to further improve the properties of the magnetic metal particles containing iron as a main component and achieve a better economy.

As methods for improving various properties of magnetic metal particles, there are known (1) techniques of specifying the composition of magnetic metal particles (Japanese Patent Application Laid-Open (KOKAI) Nos. 7-210856, 8-279142, 9-293233, 9-295814, 10-69629, 10-245233, 10-275326, 10-334455, 10-334457, 11-11951, 11-130439 and 11-251122); (2) techniques of controlling the BET specific surface area to a low value (Japanese Patent Publication (KOKOKU) No. 1-18961 and Japanese Patent Application Laid-Open (KOKAI) No. 8-236327); (3) techniques for obtaining magnetic metal particles containing iron as a main component which are uniform in properties and can show a high coercive force, by forming a fixed-bed of particles and heat-treating the fixed-bed (Japanese Patent Application Laid-Open (KOKAI) Nos. 54-62915, 4-224609 and 6-93312); or the like.

At present, it has been strongly required to provide spindle-shaped magnetic metal particles containing iron as a main component which can exhibit not only an adequate coercive force of 111.4 to 159.2 kA/m (1,400 to 2,000 Oe), but also good dispersibility, good oxidation stability and excellent coercive force distribution, despite fine particles, especially notwithstanding the average major axis diameter thereof is as small as 0.05 to 0.15 μm. However, such spindle-shaped magnetic metal particles containing iron as a main component have not been obtained conventionally.

Namely, in the above techniques (1) of specifying the composition of magnetic metal particles as described in the above KOKAIs, although the contents of Co, Al and rare earth element based on whole Fe are specified, there are no descriptions concerning the relationship between major axis diameter, specific surface area and crystallite size of the particles. The magnetic metal particles fail to satisfy all of the requirements, i.e., all of adequate coercive force, and excellent dispersibility and oxidation stability at the same time in spite of fine particles.

In particular, in Japanese Patent Application Laid-Open (KOKAI) No. 8-306031(1996), the oxidation stability of magnetic metal particles is not taken into consideration. Also, the magnetic metal particles show a poor oxidation stability because the BET specific surface area value is large relative to the average major axis diameter.

In addition, as to the above techniques (2) of controlling the BET specific surface area to a low value, in Japanese Patent Publication (KOKOKU) No. 1-18961(1989), there is disclosed the method of obtaining magnetic metal particles containing iron as a main component having an aimed coercive force and a low specific surface area by appropriately selecting the particle size and aspect ratio, thereby reducing a viscosity of a coating composition containing the particles. However, in this method, neither oxidation stability of the magnetic metal particles containing iron as a main component nor squareness and orientation property of coating film are taken into consideration. Further, in Japanese Patent Application Laid-Open (KOKAI) No. 8-236327(1986), there is described the method of precipitating metal hydrate or metal oxide simultaneously with surface oxidation of magnetic metal particles containing iron as a main component. However, in this method, the crystallite size of the particles is not taken into consideration. Further, since the coercive force of magnetic coating film is considerably different from that of the magnetic metal particles containing iron as a main component, it will be difficult to produce magnetic recording medium having aimed magnetic properties.

Further, as to the techniques (3) of obtaining magnetic metal particles containing iron as a main component by forming a fixed-bed of starting particles, in Japanese Patent Application Laid-Open (KOKAI) No. 4-224609(1992), although it is described that the atmosphere used upon heating is hydrogen, no temperature-rising rate is specified therein. Therefore, in this KOKAI, oxidation stability of the magnetic metal particles containing iron as a main component is not sufficiently considered. Also, in the method described in Japanese Patent Application Laid-Open (KOKAI) No. 54-62915(1979), magnetic metal particles containing iron as a main component obtained therein exhibit a coercive force as low as about 95.5 kA/m (1,200 Oe) probably because of nitrogen atmosphere used upon heating and low superficial velocity of reducing gas. Further, in this method, the dispersibility in coating composition as well as squareness and orientation property of coating film are not sufficiently considered. Furthermore, in the method described in Japanese Patent Application Laid-Open (KOKAI) No. 6-93312(1994), since no cobalt is incorporated into the particles, the oxidation stability of magnetic particles, the dispersibility in coating composition, the squareness and orientation property of coating film, etc., are not sufficiently considered.

The magnetic metal particles described in Japanese Patent Application Laid-Open (KOKAI) No. 2000-302445 show an excellent oxidation stability. However, it has been required to provide magnetic metal particles exhibiting a more excellent oxidation stability despite a less cobalt content.

As a result of the present inventors' earnest studies for solving the above problems, it has been found that by adding a Co compound in an amount of from 0.5 to less than 5 atm % (calculated as Co) based on whole Fe, to a water suspension containing a ferrous-containing precipitate during aging but prior to the elapse of 50% of the whole aging time before initiation of oxidation reaction; conducting the oxidation reaction such that 30 to 50% of whole Fe²⁺ is oxidized while passing an oxygen-containing gas through the water suspension at a superficial velocity of 2.3 to 3.5 cm/s; after adding an Al compound in an amount of from 5 to 10 atm % (calculated as Al) based on whole Fe, to the water suspension, successively conducting the oxidation reaction, thereby obtaining spindle-shaped goethite particles; adding a rare earth compound in an amount of 1.5 to 5 atm % (calculated as rare earth element) based on whole Fe together with Co in an amount of 20 to 200% based on whole Co contained in the spindle-shaped goethite particles produced the above and in an amount of from 5 to less than 15 atm % based on whole Fe, to the water suspension containing the obtained spindle-shaped goethite particles to form a surface coat thereon; heat-treating the spindle-shaped goethite particles at a temperature of 650 to 800° C. in a non-reducing atmosphere, thereby obtaining spindle-shaped hematite particles; introducing the obtained spindle-shaped hematite particles into a reducing apparatus to form a fixed-bed thereof having a height of 3 to 15 cm, heating the fixed-bed to a temperature of 400 to 700° C. at a temperature-rising rate of 10 to 80° C./minute in an atmosphere of a reducing gas flowed therethrough at a superficial velocity of 40 to 150 cm/s to reduce the spindle-shaped hematite particles, and forming a surface oxide coat on the resultant particles,

the thus obtained spindle-shaped magnetic metal particles containing iron as a main component can exhibit not only adequate coercive force, good dispersibility and good oxidation stability, but also excellent coercive force distribution. The present invention has been attained on the basis of this finding.

SUMMARY OF THE INVENTION

An object of the present invention is to provide spindle-shaped magnetic metal particles containing iron as a main component which can exhibit not only adequate coercive force, good dispersibility and good oxidation stability, but also excellent coercive force distribution despite fine particles, especially notwithstanding the average major axis diameter thereof is as small as 0.05 to 0.15 μm.

Another object of the present invention is to provide a process for producing spindle-shaped magnetic metal particles containing iron as a main component which are fine particles having an average major axis diameter of 0.05 to 0.15 μm, and can exhibit not only adequate coercive force, good dispersibility and good oxidation stability, but also excellent coercive force distribution, using a reducing apparatus in which a fixed-bed of the particles is formed.

To the accomplish the aim, in a first aspect of the present invention, there are provided spindle-shaped magnetic metal particles containing iron as a main component, having an average major axis diameter (L) of 0.05 to 0.15 μm; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of from 150 to less than 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula:

S≦−160×L+65;

an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.

In a second aspect of the present invention, there are provided spindle-shaped magnetic metal particles containing iron as a main component, having an average major axis diameter (L) of 0.05 to 0.15 μm; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of from 150 to less than 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula:

S≦−160×L+65;

an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.,

which are produced by heat-dehydrating spindle-shaped goethite particles to obtain spindle-shaped hematite particles and then heat-reducing the spindle-shaped hematite particles,

said spindle-shaped goethite particle comprising a spindle-shaped goethite seed crystal particle containing Co, a goethite layer formed on the surface of the spindle-shaped goethite seed crystal particle, containing Co and Al, and a surface layer form on the goethite layer, comprising rare earth compounds,

a cobalt content in the spindle-shaped goethite seed crystal particle being from 0.5 to less than 5 atm % based on whole Fe contained in the spindle-shaped goethite particle; an Al content in the goethite layer being from 5 to 10 atm % based on whole Fe contained in the spindle-shaped goethite particle; an Co content in the surface layer being 20 to 200% based on whole Co contained in the spindle-shaped goethite seed crystal particle containing Co and the goethite layer, and being from 5 to less than 15 atm % based on whole Fe; and the rare earth content in the surface layer being 1.5 to 5 atm % based on whole Fe contained in the spindle-shaped goethite particle.

In a third aspect of the present invention, there are provided spindle-shaped magnetic metal particles containing iron as a main component, having an average major axis diameter (L) of 0.05 to .0.15 μm; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of from 150 to less than 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula:

S≦−160×L+65;

an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.,

which are produced by heat-reducing spindle-shaped hematite particles,

said spindle-shaped hematite particle comprising a spindle-shaped hematite particle containing Co, a hematite layer formed on the surface of the spindle-shaped hematite particle, containing Co and Al, and a surface layer form on the hematite layer, comprising rare earth compounds,

a cobalt content in the spindle-shaped hematite core particle being from 0.5 to less than 5 atm % based on whole Fe contained in the spindle-shaped hematite particle; an Al content in the hematite layer being from 5 to 10 atm % based on whole Fe contained in the spindle-shaped hematite particle; an Co content in the surface layer being 20 to 200% based on whole Co contained in the spindle-shaped hematite core particle containing Co and the hematite layer, and being from 5 to less than 15 atm % based on whole Fe; and the rare earth content in the surface layer being 1.5 to 5 atm % based on whole Fe contained in the spindle-shaped hematite particle.

In a fourth aspect of the present invention, there is provided a process for producing spindle-shaped magnetic metal particles containing iron as a main component, comprising:

a first step comprising: aging a water suspension containing a ferrous-containing precipitate produced by reacting a mixed aqueous alkali solution comprising an aqueous alkali carbonate solution and an aqueous alkali hydroxide solution with an aqueous ferrous salt solution, in a non-oxidative atmosphere; conducting an oxidation reaction of the water suspension by passing an oxygen-containing gas therethrough, thereby producing spindle-shaped goethite seed crystal particles; and passing again an oxygen-containing gas through the water suspension containing both the ferrous-containing precipitate and the spindle-shaped goethite seed crystal particles so as to conduct an oxidation reaction thereof, thereby forming a goethite layer on the surface of the seed crystal particles to obtain spindle-shaped goethite particles,

upon the production of said seed crystal particles, a Co compound being added in an amount of from 0.5 to less than 5 atm %, calculated as Co, based on whole Fe, to the water suspension containing the ferrous-containing precipitate during the aging thereof but prior to the elapse of 50% of the whole aging time before initiation of the oxidation reaction; the oxidation reaction being conducted while passing the oxygen-containing gas through the water suspension at a superficial velocity of 2.3 to 3.5 cm/s such that 30 to 50% of whole Fe²⁺ is oxidized; an Al compound being added in an amount of 5 to 10 atm %, calculated as Al, based on whole Fe; and the oxidation reaction being successively conducted to obtain spindle-shaped goethite particles;

a second step comprising adding an anti-sintering agent containing a rare earth compound in an amount of 1.5 to 5 atm %, calculated as a rare earth element, based on whole Fe and a Co compound in an amount of 20 to 200% based on whole Co contained in the spindle-shaped goethite seed crystal particle containing Co and the goethite layer containing Co, and being from 5 to less than 15 atm % based on whole Fe contained in the spindle-shaped goethite particle;

a third step comprising heat-treating the thus treated spindle-shaped goethite particles at a temperature of 650 to 800° C. in a non-reducing atmosphere, thereby obtaining spindle-shaped hematite particles; and

a fourth step comprising charging the spindle-shaped hematite particles obtained in the above third step into a reducing apparatus to form a fixed-bed having a height of 3 to 15 cm; heating the fixed-bed of the spindle-shaped hematite particles to a temperature of 400 to 700° C. at a temperature-rising rate of 10 to 80° C./minute in an atmosphere of a reducing gas passed though the reducing apparatus at a superficial velocity of 40 to 150 cm/s, thereby reducing the spindle-shaped hematite particles; and then forming an oxide coating film on the surface of the thus reduced particles, thereby obtaining the magnetic metal particles containing iron as a main component.

In a fifth aspect of the present invention, there is provided a magnetic recording medium comprising a non-magnetic substrate and a magnetic recording layer formed on the non-magnetic substrate comprising a binder resin and spindle-shaped magnetic metal particles containing iron as a main component, which have an average major axis diameter (L) of 0.05 to 0.15 μm; a coercive force of 111.4 to 143.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of 150 to 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula:

S≦−160×L+65;

an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.

In a sixth aspect of the present invention, there is provided a magnetic recording medium comprising a non-magnetic base film; a non-magnetic undercoat layer formed on said non-magnetic base film; and a magnetic recording layer formed on the non-magnetic substrate comprising a binder resin and spindle-shaped magnetic metal particles containing iron as a main component, which have an average major axis diameter (L) of 0.05 to 0.15 μm; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of 150 to 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula:

S≦−160×L+65;

an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.

In a seventh aspect of the present invention, there are provided spindle-shaped magnetic metal particles containing iron as a main component, having an average major axis diameter (L) of 0.05 to 0.15 μm; a size distribution (standard deviation/average major axis diameter) of not more than 0.30; an aspect ratio of 4:1 to 8:1; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; an Al content of from 5 to 10 atm % based on whole Fe; a rare earth element content of from 1.5 to 5 atm % based on whole Fe; a crystallite size of from 150 to less than 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula:

S≦−160×L+65;

an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.

DETAILED DESCRIPTION OF THE INVENTION

First, the spindle-shaped magnetic metal particles containing iron as a main component according to the present invention are described below.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention contain Co in an amount of usually from 5 to less than 15 atm %, preferably from 5.5 to 14.5 based on whole Fe. When the Co content is less than 5 atm %, the effect of more improving magnetic properties may not be sufficiently exhibited. When the Co content is not less than 15 atm %, it may be difficult to retain the particle shape upon the reduction because of the reduction-promoting effect of Co. Therefore, in such a case, it is necessary to increase the rare earth element content, resulting in economically disadvantageous process.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention also contain Al in an amount of usually from 5 to 10 atm %, preferably from 5.5 to 9.5 atm % based on whole Fe; and a rare earth element in an amount of usually from 1.5 to 5 atm %, preferably from 2.0 to 4.8 atm % based on whole Fe. An atomic ratio value of Al to Co is usually from 0.3 to less than 2.0, preferably 0.4 to 1.5.

When the Al content is less than 5 atm %, it may be difficult to adequately control a coercive force of the obtained particles, especially those particles having a small particle size, since the coercive force becomes too large. When the Al content is more than 10 atm %, it also may become difficult to attain a well-controlled coercive force because the particles have a relatively low aspect ratio. When the rare earth content is less than 1.5 atm %, a sufficient anti-sintering effect may not be obtained. Further, the obtained magnetic metal particles may be deteriorated in size distribution, resulting in deteriorated SFD of magnetic coating film obtained therefrom. When the rare earth content is more than 5 atm %, the saturation magnetization of the obtained particles is considerably reduced. When the atomic ratio value of Al to Co is not less than 2, it also may become difficult to attain a well-controlled coercive force because the particles have a relatively low aspect ratio.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention have an average major axis diameter of usually from 0.05 to less than 0.15 μm, preferably 0.06 to 0.14 μm. When the average major axis diameter is less than 0.05 μm, the obtained magnetic metal particles have a too small particle size and, therefore, may tend to be deteriorated in saturation magnetization and coercive force as well as dispersibility in coating composition, so that the oxidation stability of the magnetic coating film obtained therefrom may tend to be deteriorated. When the average major axis diameter is not less than 0.15 μm, it may be difficult to obtain the aimed coercive force. In addition, since the particle size becomes too large, the obtained magnetic coating film may tend to be deteriorated in surface smoothness, resulting in poor output characteristics thereof.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention have a crystallite size D₁₁₀ of usually from 150 to less than 170 Å, preferably 150 to 165 Å. When the crystallite size D₁₁₀ is less than 150 Å, although the noise of obtained magnetic recording media due to the particles is suitably reduced, the magnetic recording media may tend to be deteriorated in saturation magnetization and oxidation stability. When the crystallite size D₁₁₀ is not less than 170 Å, the noise due to the particles may be increased.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention have a BET specific surface area (S) satisfying the formula:

S≦−160×L+65

wherein L represents an average major axis diameter of the particles.

When the BET specific surface area exceeds the value calculated from the above formula, the obtained magnetic metal particles containing iron as a main component fail to show an excellent oxidation stability. The lower limit of the BET specific surface area is preferably 30 m²/g. When the BET specific surface area is less than 30 m²/g, the obtained magnetic metal particles may be already sintered upon the previous heat-reduction treatment, so that it may become difficult to improve the squareness of the magnetic coating film obtained therefrom.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention have a size distribution (standard deviation/average major axis diameter) of usually not more than 0.30, preferably 0.10 to 0.25. The size distribution of the spindle-shaped magnetic metal particles containing iron as a main component according to the present invention is preferably as small as possible. Although the lower limit of the size distribution is not particularly restricted, in the consideration of industrial productivity, the lower limit of the size distribution is suitably about 0.10. When the size distribution is more than 0.30, the obtained particles may tend to be deteriorated in oxidation stability, so that the magnetic coating film obtained therefrom may tend to be deteriorated in SFD, thereby failing to attain a high density recording performance thereof.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention have an aspect ratio of usually 4:1 to 8:1, preferably 5:1 to 8:1. When the aspect ratio is less than 4:1, there is a tendency that the spindle-shaped magnetic metal particles cannot show the aimed coercive force, and the magnetic coating film obtained therefrom may be deteriorated in both squareness ratio and orientation ratio. When the aspect ratio is more than 8:1, the obtained particles may tend to exhibit a too high coercive force or be deteriorated in oxidation stability.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention have a coercive force Hc of usually 111.4 to 159.2 kA/m (1,400 to 2,000 Oe), preferably 127.3 to 157.6 kA/m (1,600 to 1,980 Oe); and a saturation magnetization σs of usually 120 to 150 Am²/kg (120 to 150 emu/g), preferably 120 to 140 Am²/kg (120 to 140 emu/g).

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention have an oxidation stability (Δσs) of saturation magnetization (σs) of usually not more than 4.5%, preferably 0.5 to 4.5%, as an absolute value, and an ignition temperature of usually not less than 145° C., preferably 145 to 185° C., when measured after one-week accelerated deterioration test at a temperature of 60° C. and a relative humidity of 90%. When the oxidation stability of saturation magnetization and the ignition temperature is out of the above-specified range, the obtained particles fail to show a sufficient oxidation stability.

As to properties of a coating film produced using the spindle-shaped magnetic metal particles containing iron as a main component according to the present invention, when the coating film is oriented by applying a magnetic field of 397.9 kA/m (5 kOe) thereto, the squareness (Br/Bm) thereof is usually not less than 0.84; the orientation property (OR) thereof is usually not less than 2.8; and the coercive force distribution (SFD) thereof is usually not more than 0.53.

The magnetic coating film produced using the spindle-shaped magnetic metal particles containing iron as a main component according to the present invention, have an oxidation stability (ΔBm) of usually not more than 3.5%, preferably 0.3 to 3.5%, when the magnetic coating film is oriented by applying a magnetic field of 397.9 kA/m (5 kOe) thereto.

Next, the process for producing the spindle-shaped magnetic metal particles containing iron as a main component according to the present invention is described below.

The spindle-shaped magnetic metal particles of the present invention can be produced by the process comprising the first step of producing spindle-shaped goethite particles; the second step of forming a surface coat on the spindle-shaped goethite particles to obtain starting particles; the third step of heat-dehydrating the starting particles to obtain spindle-shaped hematite particles; and the fourth step of heat-reducing the spindle-shaped hematite particles.

The first step of producing the spindle-shaped goethite particles is described below.

The spindle-shaped goethite particles are produced by forming spindle-shaped goethite seed crystal particles and then growing a goethite layer on the surface of respective goethite seed crystal particles.

The production conditions of spindle-shaped goethite seed crystal particles are as follows. That is, upon the production of the spindle-shaped goethite seed crystal particles by reacting an aqueous ferrous salt solution with a mixed aqueous alkali solution of an aqueous alkali carbonate solution and an aqueous alkali hydroxide solution to form a water suspension containing a ferrous-containing precipitate; aging the resultant water suspension in a non-oxidative atmosphere; and then passing an oxygen-containing gas through the water suspension to conduct an oxidation reaction thereof, a Co compound is added in an amount of usually from 0.5 to less than 5 atm % (calculated as Co) based on whole Fe, to the water suspension containing the ferrous-containing precipitate during aging of the water suspension but prior to the elapse of 50% of the whole aging time before initiation of the oxidation reaction, and then the oxidation reaction is conducted such that usually 30 to 50% of whole Fe²⁺ contained in spindle-shaped goethite particles is oxidized.

When the Co compound is added after the elapse of 50% of the whole aging time, the obtained goethite particles fail to show the aimed particle size and aspect ratio. In addition, when the oxidation percentage of whole Fe²⁺ upon the oxidation reaction is less than 30% and more than 50%, it may be also difficult to obtain goethite particles having the aimed particle size and aspect ratio.

The aging of the water suspension is preferably conducted at a temperature of 40 to 80° C. in a non-oxidative atmosphere. When the aging temperature is less than 40° C., a sufficient aging effect may not be attained, so that the obtained particles may have a small aspect ratio. When the aging temperature is more than 80° C., magnetite particles tend to be mixed in the aimed goethite seed crystal particles. The aging time is usually 30 to 300 minutes. When the aging time is less than 30 minutes and more than 300 minutes, it may become difficult to obtain particles having the aimed aspect ratio. In order to produce the non-oxidative atmosphere, an inert gas such as nitrogen or a reducing gas such as hydrogen may be passed though a reactor containing the water suspension.

As the aqueous ferrous salt solution used in the production reaction of the spindle-shaped goethite seed crystal particles, there may be used an aqueous ferrous sulfate solution, an aqueous ferrous chloride solution or the like. These solutions may be used singly or in the form of a mixture of any two or more thereof.

The mixed aqueous alkali solution used in the production reaction of the spindle-shaped goethite seed crystal particles may be produced by mixing an aqueous alkali carbonate solution with an aqueous alkali hydroxide solution. The mixing ratio between the alkali hydroxide and the alkali carbonate (% calculated as normality) is adjusted such that the concentration of the alkali hydroxide is preferably 10 to 40%, more preferably 15 to 35% (calculated as normality). When the concentration of the alkali hydroxide contained in the mixed aqueous solution is less than 10%, there is a tendency that particles having the aimed aspect ratio may not be obtained. When the concentration of the aqueous alkali hydroxide solution is more than 40%, granular magnetite particles may tend to be mixed in the aimed spindle-shaped goethite seed crystal particles.

As the aqueous alkali carbonate solution, there may be used an aqueous sodium carbonate solution, an aqueous potassium carbonate solution, an aqueous ammonium carbonate solution or the like. As the aqueous alkali hydroxide solution, there may be used an aqueous sodium hydroxide solution, an aqueous potassium hydroxide solution or the like. These solutions may be respectively used singly or in the form of a mixture of any two or more thereof.

As to the amount of the mixed aqueous alkali solution used, the equivalent ratio of alkali contained therein to whole Fe contained in the aqueous ferrous salt solution, is usually 1.3:1 to 3.5:1, preferably 1.5:1 to 2.5:1. When the equivalent ratio is less than 1.3:1, magnetite particles may tend to be mixed in the aimed spindle-shaped goethite particles. When the equivalent ratio is more than 3.5:1, the use of such a large equivalent ratio is industrially disadvantageous.

The ferrous concentration of the solution obtained by mixing the aqueous ferrous salt solution with the mixed aqueous alkali solution is usually 0.1 to 1.0 mol/liter, preferably 0.2 to 0.8 mol/liter. When the ferrous concentration is less than 0.1 mol/liter, the yield of the aimed particles may be lowered, resulting in industrially disadvantageous process. When the ferrous concentration is more than 1.0 mol/liter, the particle size distribution of the obtained particles may become too broad.

The pH value of the solution used in the production reaction of the spindle-shaped goethite seed crystal particles is usually 8.0 to 11.5, preferably 8.5 to 11.0. When the pH value is less than 8.0, a large amount of acid radicals may be contained in the obtained goethite particles. Since the acid radicals cannot be simply removed by ordinary washing method, the goethite particles may tend to be sintered together when heat-treated to form the magnetic metal particles. When the pH value is more than 11.5, the obtained particles may tend to fail to exhibit the aimed coercive force.

The production reaction of the spindle-shaped goethite seed crystal particles is conducted by the oxidation reaction, more specifically, by passing an oxygen-containing gas such as air through the solution.

The superficial velocity of the oxygen-containing gas is usually 2.3 to 3.5 cm/s, preferably 2.3 to 3.3 cm/s. When the superficial velocity is less than 2.3 cm/s, the oxidation velocity is low, so that granular magnetite particles may tend to be mixed in the aimed spindle-shaped seed crystal particles, and it may become difficult to control the particles size as required. When the superficial velocity is more than 3.5 cm/s, the oxidation velocity is too high, so that it may become difficult to control the particle size as required. Here, the “superficial velocity” means an amount of the oxygen-containing gas passed through the reactor per its unit sectional area (bottom sectional area of a cylindrical reactor where the pore diameter and pore number of a perforated plate are ignored; unit: cm/sec).

The production reaction of the spindle-shaped goethite seed crystal particles may be conducted at a temperature of usually not more than 80° C. at which goethite particles may be ordinarily produced. When the reaction temperature is more than 80° C., magnetite particles may tend to be mixed in the aimed spindle-shaped goethite particles. The reaction temperature is preferably 45 to 55° C.

As the Co compound added in the production reaction of the spindle-shaped goethite seed crystal particles, there may be used cobalt sulfate, cobalt chloride, cobalt nitrate or the like. These Co compounds may be used alone or in the form of a mixture of any two or more thereof. The Co compound is added to the water suspension containing the ferrous-containing precipitate during the aging time thereof before initiation of the oxidation reaction.

The amount of the Co compound added is usually from 0.5 to less than 5 atm % based on whole Fe contained in the spindle-shaped goethite particles as a final product.

The pH value of the water suspension used in the growth reaction of the goethite layer is usually 8.0 to 11.5, preferably 8.5 to 11.0. When the pH value is less than 8.0, a large amount of acid radicals may be contained in the obtained goethite particles. Since such acid radicals cannot be simply removed by ordinary washing method, the goethite particles may tend to be sintered together when heat-treated to form magnetic metal particles. When the pH value is more than 11.5, it may tend to be difficult to obtain particles having the aimed particle size distribution.

The growth of the goethite layer is conducted by the oxidation reaction, more specifically, by passing an oxygen-containing gas such as air though the water suspension. The superficial velocity of the oxygen-containing gas used in the growth reaction of the goethite layer is preferably larger than that used in the production reaction of the seed crystal particles, in the range of usually from more than 2.3 to 3.5 cm/s. When the superficial velocity used in the growth reaction of the goethite layer is not larger than that used in the production reaction of the seed crystal particles, the viscosity of the water suspension may be increased upon adding Al thereto. As a result, the growth in the minor axis direction is more remarkably accelerated, so that the aspect ratio may be decreased, thereby failing to obtain particles having the aimed aspect ratio.

The growth reaction of the goethite layer may be conducted at a temperature of usually not more than 80° C. at which goethite particles can be produced. When the growth reaction temperature is more than 80° C., magnetite particles may tend to be mixed in the aimed goethite particles. The growth reaction temperature is preferably 45 to 55° C.

As the Al compound added in the growth reaction of the goethite layer, there may be used acid salts such as aluminum sulfate, aluminum chloride and aluminum nitrate; and aluminates such as sodium aluminate, potassium aluminate and ammonium aluminate. These Al compounds may be used alone or in the form of a mixture of any two or more thereof.

In the growth reaction of the goethite layer, the addition of the Al compound may be conducted simultaneously with passing the oxygen-containing gas through the water suspension at such a superficial velocity preferably larger than that used in the production reaction of the seed crystal particles in the range of usually from more than 2.3 to 3.5 cm/s.

When the addition of the Al compound requires a long period of time, the oxygen-containing gas may be replaced with a nitrogen-containing gas so as not to accelerate the oxidation reaction. Meanwhile, in the above case, when the Al compound is added in separate parts, continuously or intermittently while passing the oxygen-containing gas through the water suspension, it is not possible to sufficiently attain the effects of the present invention.

The amount of the Al compound added is usually from 5 to 10 atm %, preferably 5.5 to 9.5 atm % based on whole Fe contained in the spindle-shaped goethite particles as a final product.

The thus obtained spindle-shaped goethite particles have a cobalt content of usually from 0.5 to less than 5 atm %, preferably from 1.0 to 4.8 atm % based on whole Fe, and an Al content of usually from 5 to 10 atm %, preferably from 5.5 to 9.5 atm % based on whole Fe.

When the Co content of the spindle-shaped goethite particles is less than 0.5 atm %, the effect of improving magnetic properties cannot be obtained when the magnetic metal particles are produced therefrom. When the Co content is not less than 5 atm %, it may be difficult to adequately control the particle size, and the use of such a large amount of Co is economically disadvantageous. When the Al content is less than 5 atm %, although the anti-sintering effect is attained, the coercive force of the obtained particles, especially those having a small particle size, may become too large, thereby failing to adequately control the coercive force. When the Al content is more than 10 atm %, it may be difficult to adequately control the coercive force because the particles have a relatively small aspect ratio.

The spindle-shaped goethite particles used in the present invention are of a spindle shape, and have an average major axis diameter of usually 0.05 to 0.18 μm, preferably 0.07 to 0.17 μm; a size distribution (standard deviation/average major axis diameter) of usually not more than 0.20, preferably 0.10 to 0.196; and an aspect ratio (average major axis diameter/average minor axis diameter) of usually from 4:1 to 8:1, preferably 5:1 to 8:1.

When the average major axis diameter of the spindle-shaped goethite particles is less than 0.05 μm, the magnetic metal particles obtained therefrom have a too small particle size and, therefore, may tend to be deteriorated in saturation magnetization, coercive force, dispersibility in coating composition, and oxidation stability. When the average major axis diameter of the spindle-shaped goethite particles is more than 0.18 μm, it may be difficult to obtain the aimed coercive force. Further, the obtained coating film may tend to be deteriorated in surface smoothness due to the large particle size, thereby failing to improve the output characteristics thereof.

The spindle-shaped goethite particles preferably have a size distribution as small as possible. Although the lower limit of the size distribution of the spindle-shaped goethite particles is not particularly restricted, in the consideration of industrial productivity, the lower limit thereof is preferably about 0.10. When the size distribution of the spindle-shaped goethite particles is more than 0.20, the magnetic metal particles obtained therefrom may tend to be deteriorated in oxidation stability, thereby failing to achieve a high density recording performance of magnetic recording media. When the aspect ratio of the spindle-shaped goethite particles is less than 4:1, the aimed coercive force may not be obtained. When the aspect ratio is more than 8:1, the obtained particles may exhibit a too high coercive force or may be deteriorated in oxidation stability.

In addition, the spindle-shaped goethite particles used in the present invention have a BET specific surface area of usually 100 to 200 m²/g, preferably 120 to 200 m²/g. When the BET specific surface area is less than 100 m²/g, the obtained spindle-shaped goethite particles are relatively large in size, so that the magnetic metal particles containing iron as a main component obtained therefrom may tend to fail to exhibit the aimed coercive force. When the BET specific surface area is more than 200 m²/g, the coercive force of the spindle-shaped magnetic metal particles containing iron as a main component obtained from the spindle-shaped goethite particles may become so high beyond required level, resulting in deteriorated oxidation stability.

The spindle-shaped goethite particles used in the present invention have a crystallite size D₀₂₀ of usually 100 to 200 Å, preferably 120 to 200 Å; a crystallite size D₁₁₀ of usually 60 to 130 Å, preferably 100 to 125 Å; and a crystallite size ratio D₀₂₀/D₁₁₀ of usually less than 1.8, preferably not more than 1.78. When the crystallite size ratio D₀₂₀/D₁₁₀ is not less than 1.8, the magnetic metal particles containing iron as a main component obtained from such goethite particles have the aimed particle size, but may tend to fail to exhibit the aimed coercive force.

The spindle-shaped goethite particles used in the present invention are each constituted by a seed crystal portion and a surface layer portion. Cobalt is present in both the seed crystal and surface layer portions, while aluminum is present only in the surface layer portion.

Here, the “seed crystal portion” means a goethite seed crystal particle produced by oxidizing a part of the ferrous salt added, prior to the addition of the Al compound. More specifically, the seed crystal portion is a portion having a specific weight percentage of Fe determined by the oxidation percentage of Fe²⁺, preferably a portion extending outwardly from the center of each goethite particle which contains Fe in an amount of 30 to 50% by weight based on whole Fe contained in the goethite particle.

Next, the second step of producing the spindle-shaped hematite particles is described below.

In the present invention, the spindle-shaped goethite particles are coated with the rare earth compound and Co, thereby obtaining starting particles.

Examples of the suitable rare earth compounds may include compounds of at least one element selected from the group consisting of scandium, yttrium, lanthanum, cerium, praseodymium, neodymium and samarium. Also, there may be used such rare earth compounds in the form of chlorides, sulfates, nitrates or the like. The coating of the rare earth compound may be conducted by either dry or wet method. Of these methods, the use of wet coating method is preferred.

The amount of the rare earth compound used is usually 1.5 to 5 atm %, preferably 2.0 to 4.8 atm % based on whole Fe.

The amount of Co used in the coating is 20 to 200% based on a whole amount of Co contained in the spindle-shaped goethite particles produced at the first step. When the amount of Co used is more than 200%, it may be difficult to uniformly coat the spindle-shaped goethite particles therewith because of a too large amount of Co, so that an isolated Co compound may tend to be precipitated. Further, the magnetic metal particles produced from such particles may tend to suffer from deteriorated magnetic properties. When the amount of Co used is less than 20%, it may be difficult to obtain the effect of the present invention because the amount of Co coated is too small.

When the rare earth compound and Co are coated simultaneously, the sintering within particles and between particles can be prevented, thereby enabling the production of spindle-shaped hematite particles more analogously. retaining the shape and aspect ratio of the spindle-shaped goethite particles. Further, this facilitates the production of spindle-shaped magnetic metal particles containing iron as a main component which are independent particles and can retain the shape and the like of the starting particles.

The starting particles are each constituted by a goethite seed crystal particle, a goethite layer and an outer layer. Co is present in the goethite seed crystal particle, the goethite layer and the outer layer, while Al is present only in the goethite layer and the rare earth element is present only in the outer layer.

Since Co is also present in the outer layer, it becomes possible to obtain magnetic metal particles containing iron as a main component capable of exhibiting an excellent oxidation stability despite a less Co content.

The third step of heat-dehydrating the starting particles is described below.

The spindle-shaped hematite particles can be produced by heat-treating the starting particles obtained in the second step, at a temperature of 650 to 800° C. in a non-reducing atmosphere.

The heat-treatment of the starting particles at a temperature of 650 to 800° C. in a non-reducing atmosphere is preferably conducted such that the crystallite size ratio: D₁₀₄(hematite)/D₁₁₀(goethite) lies within the range of 1.0 to 1.3.

When the heat-treating temperature is less than 650° C., the crystallite size ratio: D₁₀₄(hematite)/D₁₁₀(goethite) may tend to become less than 1.0. As a result, the magnetic metal particles obtained from such spindle-shaped hematite particles may tend to show a broad particle size distribution, so that the coating film produced therefrom may tend to be deteriorated in SFD. When the heat-treating temperature is more than 800° C., the crystallite size ratio: D₁₀₄(hematite)/D₁₁₀(goethite) may tend to be more than 1.3. Therefore, the obtained hematite particles may tend to suffer from shape breakage and sintering. As a result, the magnetic metal particles obtained from such hematite particles also may tend to show a broad particle size distribution and include sintered portions therein, and the magnetic coating film produced therefrom may tend to be deteriorated in both squareness and SFD.

After the heat-treatment, the obtained hematite particles may be rinsed in order to remove impurity salts such as Na₂SO₄ therefrom. In this case, the rinsing is preferably conducted so as to remove only undesired impurity salts without elution of the anti-sintering agent coated. More specifically, the rinsing can be effectively performed under a high pH condition in order to remove cationic impurities, and under a low pH condition in order to remove anionic impurities.

The thus obtained spindle-shaped hematite particles contain Co in an amount of usually from 5 to less than 15 atm %, preferably from 5.5 to 14.5 atm % based on whole Fe; Al in an amount of usually from 5 to 10 atm %, preferably from 5.5 to 9.5 atm % based on whole Fe; and a rare earth element in an amount of usually from 1.5 to 5 atm %, preferably from 2.0 to 4.8 atm % based on whole Fe. The reasons why the Al and Co contents of the spindle-shaped hematite particles are defined to the above ranges, are the same as those described above as to the Al and Co contents of the goethite particles. When the rare earth element content of the spindle-shaped hematite particles is less than 1.5 atm %, a sufficient anti-sintering effect may not be obtained. As a result, the magnetic metal particles obtained from such hematite particles may be deteriorated in size distribution, and further the magnetic coating film produced therefrom may be deteriorated in SFD. When the rare earth element content is more than 5 atm %, the saturation magnetization of the obtained particles may be remarkably deteriorated.

The spindle-shaped hematite particles used in the present invention are of a spindle shape, and have an average major axis diameter of usually 0.05 to 0.17 μm, preferably 0.07 to 0.17 μm; a size distribution (standard deviation/average major axis diameter) of usually not more than 0.22, preferably 0.10 to 0.21; and an aspect ratio of usually from 4:1 to 9:1, preferably 5:1 to 9:1.

When the average major axis diameter of the spindle-shaped hematite particles is less than 0.05 μm, the magnetic metal particles obtained therefrom have a too small particle size and, therefore, may tend to be deteriorated in saturation magnetization and coercive force, dispersibility in coating composition and oxidation stability. When the average major axis diameter of the spindle-shaped hematite particles is more than 0.17 μm, it may be difficult to attain the aimed coercive force when the aspect ratio lies within the above-specified range. In addition, since the particle size becomes too large, the obtained magnetic coating film may tend to be deteriorated in surface smoothness, resulting in poor output characteristics thereof.

The spindle-shaped hematite particles used in the present invention preferably have a size distribution as small as possible. Although the lower limit of the size distribution is not particularly restricted, in the consideration of industrial productivity, the lower limit is preferably about 0.10. When the size distribution of the spindle-shaped.hematite particles is more than 0.22, the obtained particles may tend to be deteriorated in oxidation stability, thereby failing to obtain magnetic recording media having a high density recording performance. When the aspect ratio is less than 4:1, the aimed coercive force may not be obtained. When the aspect ratio is more than 9, the obtained particles may tend to exhibit a too high coercive force or be deteriorated in oxidation stability.

The spindle-shaped hematite particles used in the present invention have a BET specific surface area of usually from 35 to less than 60 m²/g, more preferably 35 to 55 m²/g. When the BET specific surface area is less than 35 m²/g, the obtained hematite particles having the particle size specified by the present invention are already sintered upon the heat-treatment and, therefore, may tend to be deteriorated in size distribution. As a result, the magnetic metal particles obtained from such hematite particles also may tend to be deteriorated in size distribution, and further the magnetic coating film produced using the magnetic metal particles tend to be deteriorated in SFD. When the BET specific surface area is not less than 60 m²/g, the anti-sintering effect may become insufficient upon the heat-reduction treatment. As a result, the magnetic metal particles obtained from such hematite particles may tend to be deteriorated in size distribution, and further the magnetic coating film produced therefrom may tend to be deteriorated in SFD.

The spindle-shaped hematite particles used in the present invention have a crystallite size D₁₀₄ of usually 100 to 160 Å, preferably 120 to 150 Å; a crystallite size D₁lo of usually 200 to 300 Å, preferably 220 to 280 Å; and a crystallite size ratio D₁₁₀/D₁₀₄ of usually 1.8 to 2.2, more preferably 1.8 to 2.1. When the crystallite size ratio D₁₁₀/D₁₀₄ is less than 1.8, excessive crystal growth of particles may tend to be caused upon the heat-dehydration treatment. Therefore, the obtained particles may tend to be deteriorated in particle size distribution in addition to the accelerated growth in the minor axis direction. As a result, the magnetic metal particles obtained from the hematite particles may tend to be lowered in coercive force and deteriorated in dispersibility. When the crystallite size ratio D₁₁₀/D₁₀₄ of the spindle-shaped hematite particles is more than 2.2, the crystal growth upon the heat-dehydration treatment may be insufficient, so that a good shape-retention effect may not be expected upon the heat-reduction treatment. As a result, the obtained particles may tend to be deteriorated in coercive force and particle size distribution.

The spindle-shaped hematite particles of the present invention retain substantially the same layer structure and composition distribution as those of the starting particles when being transformed. Therefore, the spindle-shaped hematite particles used in the present invention are each constituted by a core crystal portion (hematite core particle), an intermediate layer portion (hematite layer) and an outer layer portion (surface layer). Cobalt is present in both the core crystal and intermediate layer portions, while aluminum is present only in the intermediate layer portion and the rare earth element is present only in the outer layer portion.

Here, the “core crystal portion” of the respective hematite particles corresponds to the seed crystal portion of the above goethite particles. The core crystal portion is preferably a portion extending outwardly from the center of each hematite particle which corresponds to such a portion containing Fe in an amount of usually 30 to 50% by weight based on whole Fe contained in each hematite particle. The “intermediate layer portion” of the respective hematite particles corresponds to the surface layer portion of the above goethite particles. The intermediate layer portion is preferably a portion extending inwardly from the inner surface of the rare earth element-containing outer layer up to the outer surface of the core crystal portion, which corresponds to such a portion containing Fe in an amount of usually 50 to 70% by weight based on whole Fe contained in each hematite particle.

In the fourth step of the process of the present invention, the spindle-shaped hematite particles are introduced into a reducing apparatus to form a fixed-bed thereof. The fixed-bed of the spindle-shaped hematite particles is heat-reduced to obtain spindle-shaped magnetic metal particles containing iron as a main component.

In the present invention, upon forming the fixed-bed, the spindle-shaped hematite particles are preferably granulated by an ordinary method to form granulated particles having an average particle size of 1 to 5 mm.

As the preferred reducing apparatus usable in the present invention for forming the fixed-bed therein, there may be exemplified a moving-type (continuous-type) reducing apparatus including a belt or tray on which the fixed-bed is formed. In the reducing apparatus of this type, the hematite particles are reduced while moving the belt or tray on which the fixed-bed thereof is formed.

The fixed-bed of the granulated spindle-shaped hematite particles has a height of usually 3 to 15 cm, preferably 4 to 14 cm. When the height of the fixed-bed is more than 15 cm, the increase of water vapor partial pressure may be caused by abrupt reduction of the spindle-shaped hematite particles located at lower portion of the fixed-bed. This causes problems such as deterioration in coercive force of the particles located at an upper portion of the fixed-bed, resulting in deterioration in magnetic properties as a whole. When the height of the fixed-bed is less than 3 cm, the granulated particles may tend to be sometimes scattered around though it depends upon the superficial velocity of gas introduced.

In the present invention, the atmosphere used during heating to a reducing temperature of 400 to 700° C. is a reducing gas atmosphere. As the reducing gas, hydrogen is suitably used. If an atmosphere other than the reducing gas atmosphere, especially an inert gas atmosphere such as nitrogen, is used, abrupt reduction may tend to be caused when the atmosphere is changed over to the reducing gas atmosphere at the subsequent reducing step after heating. As a result, the uniform particle growth may be inhibited, thereby failing to attain a high coercive force.

In the present invention, the superficial velocity of the reducing gas at the above heating step is usually 40 to 150 cm/s, preferably 40 to 140 cm/s. When the superficial velocity of the reducing gas is less than 40 cm/s, the water vapor produced by the reduction of the hematite particles may be discharged out of the system at a too low velocity, thereby causing deterioration in coercive force of the particles located at an upper portion of the fixed-bed and in SFD of the coating film produced therefrom. As a result, the coercive force of the obtained particles may tend to be deteriorated as a whole. When the superficial velocity of the reducing gas is more than 150 cm/s, although the aimed spindle-shaped magnetic alloy particles can be obtained, there may tend to be caused problems such as high reducing temperature and shape breakage of the granulated particles by scattering.

In the present invention, the temperature-rising rate used upon the heating step is usually 10 to 80° C./minute, preferably 20 to 70° C./minute. When the temperature-rising rate is less than 10° C./minute, the reduction of the fixed-bed proceeds slowly from a lower portion thereof in a low temperature range. Therefore, the obtained magnetic metal particles may tend to have an extremely small crystallite size, and the water vapor produced may tend to be discharged out of the system at an extremely low velocity, resulting in deterioration in coercive force of particles located at the upper portion of the fixed-bed, SFD of the obtained coating film in addition to deterioration in crystallinity of particles located at the lower portion of the fixed-bed. As a result, it is difficult to obtain magnetic metal particles having a high coercive force as a whole. When the temperature-rising rate is more than 80° C./minute, the attitude of the heat treatment may become close to that conducted in nitrogen, thereby causing abrupt reduction as well as the transfer into α-Fe due to the relatively high water vapor partial pressure. As a result, the obtained magnetic metal particles may tend to have a large crystallite size and be deteriorated in coercive force, thereby causing deterioration in SFD of the coating film produced therefrom.

The atmosphere used in the heat-reduction of the present invention is a reducing gas atmosphere. As the reducing gas, hydrogen may be suitably used.

The heat-reducing temperature is in the range of 400 to 700° C., preferably 400 to 600° C. When the heat-reducing temperature is less than 400° C., the reduction reaction proceeds too slowly and, therefore, requires a long period of time. When the heat-reducing temperature is more than 700° C., the reduction reaction proceeds abruptly, thereby sometimes causing shape breakage of the particles and sintering within particles or between particles.

The spindle-shaped magnetic metal particles containing iron as a main component which are obtained after the heat-reduction, may be taken out in air by known methods, for example, a method of immersing the particles in an organic solvent such as toluene; a method of temporarily replacing the atmosphere around the heat-reduced spindle-shaped magnetic metal particles containing iron as a main component, with an inert gas, and then gradually increasing the oxygen content of the inert gas until the inert gas is completely replaced with air; and a method of gradually oxidizing the particles using a mixed gas of oxygen and water vapor.

Next, the magnetic recording medium according to the present invention will be described.

The magnetic recording medium according to the present invention comprises a non-magnetic substrate, and a magnetic recording layer which is formed on the non-magnetic substrate and comprising the magnetic metal particles containing iron as a main component and a binder resin.

As the non-magnetic substrate, there may be used those ordinarily used for magnetic recording media. Examples of the non-magnetic substrates may include films of synthetic resins such as polyethylene terephthalate, polyethylene, polypropylene, polycarbonates, polyethylene naphthalate, polyamides, polyamideimides and polyimides; foils or plates of metals such as aluminum and stainless steel; or various kinds of papers. The thickness of the non-magnetic substrate varies depending upon materials used, and is usually 1.0 to 300 μm, preferably 2.0 to 200 μm.

As the non-magnetic substrate for magnetic discs, there may be generally used a polyethylene terephthalate film having a thickness of usually 50 to 300 μm, preferably 60 to 200 μm As the non-magnetic substrate for magnetic tapes, there may be used a polyethylene terephthalate film having a thickness of usually 3 to 100 μm, preferably 4 to 20 μm, a polyethylene naphthalate film having a thickness of usually 3 to 50 μm, preferably 4 to 20 μm, or a polyamide film having a thickness of usually 2 to 10 μm, preferably 3 to 7 μm.

As the binder resins, there may also be used those presently ordinarily used for the production of magnetic recording media. Examples of the binder resins may include vinyl chloride-vinyl acetate copolymer resins, urethane resins, vinyl chloride-vinyl acetate-maleic acid copolymer resins, urethane elastomers, butadiene-acrylonitrile copolymer resins, polyvinyl butyral, cellulose derivatives such as nitrocellulose, polyester resins, synthetic rubber-based resins such as polybutadiene, epoxy resins, polyamide resins, polyisocyanates, electron beam-curable acrylic urethane resins, or mixtures thereof.

The respective binder resins may contain a functional group such as —OH, —COOH, —SO₃M, —OPO₂M₂ and —NH₂ wherein M represents H, Na or K. In the consideration of the dispersibility of the magnetic metal particles containing iron as a main component in vehicle upon the production of a magnetic coating composition, the use of such binder resins containing —COOH or —SO₃M as a functional group is preferred.

The thickness of the magnetic recording layer formed on the non-magnetic substrate is usually 0.01 to 5.0 μm. If the thickness is less than 0.01 μm, uniform coating may be difficult, so that unfavorable phenomenon such as unevenness on the coating surface may be observed. On the contrary, when the thickness of the magnetic recording layer is more than 5.0 μm, it may be difficult to obtain desired electromagnetic performance due to an influence of diamagnetism. The thickness of the magnetic recording layer is preferably 0.05 to 4.0 μm.

The amount of the magnetic metal particles containing iron as a main component in the magnetic recording layer is usually 5 to 2,000 parts by weight, preferably 100 to 1,000 parts by weight based on 100 parts by weight of the binder resin.

When the amount of the magnetic metal particles containing iron as a main component is less than 5 parts by weight, the magnetic metal particles containing iron as a main component may not be continuously dispersed in a coating layer due to the too small content in a magnetic coating composition, resulting in insufficient surface smoothness and strength of the obtained coating layer. When the amount of the magnetic metal particles containing iron as a main component is more than 2,000 parts by weight, the magnetic metal particles containing iron as a main component may not be uniformly dispersed in the magnetic coating composition due to the too large content as compared to that of the binder resin. As a result, when such a magnetic coating composition is coated onto the substrate, it is difficult to obtain a coating film having a sufficient surface smoothness. Further, since the magnetic metal particles containing iron as a main component cannot be sufficiently bonded together by the binder resin, the obtained coating film becomes brittle.

The magnetic recording layer may further contain various additives used in ordinary magnetic recording media such as lubricants, abrasives and anti-static agents in an amount of 0.1 to 50 parts by weight based on 100 parts by weight of the binder resin.

The magnetic recording medium of the present invention has a coercive force value of usually 111.4 to 143.2 kA/m (1,400 to 1,800 Oe), and when the magnetic coating film is oriented by applying a magnetic field of 397.9 kA/m (5 kOe) thereto, a squareness (Br/Bm) of usually not less than 0.84, an orientation property (OR) of usually not less than 2.8, a coercive force distribution (Switching Field Distribution: SFD) of usually not more than 0.53 and an oxidation stability (ΔBm) of usually not more than 3.5%.

The magnetic recording medium of the other aspect in the present invention, comprises a non-magnetic base film, a non-magnetic undercoat layer formed on the non-magnetic base film comprising a binder resin and non-magnetic particles, and a magnetic recording layer formed on the non-magnetic undercoat layer, comprising a binder resin and the spindle-shaped magnetic metal particles containing iron as a main component.

The thickness of the non-magnetic undercoat layer is preferably 0.2 to 10.0 μm. When the thickness of the non-magnetic undercoat layer is less than 0.2 μm, it may be difficult to improve the surface roughness of the non-magnetic substrate, and the stiffness of a coating film formed thereon tends to be unsatisfactory. In the consideration of reduction in total thickness of the magnetic recording medium as well as the stiffness of the coating film, the thickness of the non-magnetic undercoat layer is more preferably in the range of 0.5 to 5.0 μm.

As the binder resin, the same binder resin as that used for the production of the magnetic recording layer is usable.

The mixing ratio of the non-magnetic particles to the binder resin is usually 5 to 2000 parts by weight, preferably 100 to 1000 parts by weight based on 100 parts by weight of the binder resin.

When the content of the non-magnetic particles is as small as less than 5 parts by weight, such a non-magnetic undercoat layer in which the non-magnetic particles are uniformly and continuously dispersed may not be obtained upon coating, resulting in insufficient surface smoothness and insufficient stiffness of the non-magnetic substrate. When the content of the non-magnetic particles is more than 2,000 parts by weight, the non-magnetic particles may not be sufficiently dispersed in a non-magnetic coating composition since the amount of the non-magnetic particles is too large as compared to that of the binder resin. As a result, when such a non-magnetic coating composition is coated onto the non-magnetic base film, it may become difficult to obtain a coating film having a sufficiently smooth surface. Further, since the non-magnetic particles may not be sufficiently bonded together through the binder resin, the obtained coating film tends to become brittle.

It is possible to add an additive such as a lubricant, a polishing agent, an antistatic agent, etc. which are generally used for the production of a magnetic recording medium, to the non-magnetic undercoating layer. The mixing ratio of the additive to the binder resin is preferably 0.1 to 50 parts by weight based on 100 parts by weight of the binder resin.

As the non-magnetic particles used in the non-magnetic undercoat layer of the present invention, there may be exemplified non-magnetic inorganic particles ordinarily used for forming a non-magnetic undercoat layer in conventional magnetic recording media. Specific examples of the non-magnetic particles may include hematite particles, iron oxide hydroxide particles, titanium oxide particles, zinc oxide particles, tin oxide particles, tungsten oxide particles, silicon dioxide particles, α-alumina particles, β-alumina particles, γ-alumina particles, chromium oxide particles, cerium oxide particles, silicon carbide particles, titanium carbide particles, silicon nitride particles, boron nitride particles, calcium carbonate particles, barium carbonate particles, magnesium carbonate particles, strontium carbonate particles, calcium sulfate particles, barium sulfate particles, molybdenum disulfide particles, barium titanate particles or the like. These non-magnetic particles may be used singly or in the form of a mixture of any two or more thereof. Among them, the use of hematite particles, iron oxide hydroxide particles, titanium oxide particles or the like is preferred, and the use of hematite particles is more preferred.

In the present invention, in order to improve the dispersibility of the non-magnetic particles in vehicle upon the production of non-magnetic coating composition, the non-magnetic particles may be surface-treated with hydroxides of aluminum, oxides of aluminum, hydroxides of silicon, oxides of silicon or the like to form a coat made of any of these compounds on the surfaces thereof. Further, the non-magnetic particles may contain Al, Ti, Zr, Mn, Sn, Sb or the like inside thereof, if required, in order to improve various properties of the obtained magnetic recording media such as light transmittance, surface electrical resistivity, mechanical strength, surface smoothness, durability or the like.

The particle shape of the hematite particles as the non-magnetic particles may include a granular shape such as a spherical shape, an irregular (anisotropic) shape, an octahedral shape, a hexahedral shape, a polyhedral shape or the like; an acicular shape such as a needle shape, a spindle shape, a rice ball shape or the like; and a plate shape, or the like.

The lower limit of the average particle size of the hematite particles as the non-magnetic particles is usually 0.075 μm, preferably 0.085 μm, more preferably 0.095 μm, and the upper limit thereof is usually 0.95 μm, preferably 0.65 μm, more preferably 0.45 μm.

(i) In the case where the shape of the hematite particles is granular-shaped, the lower limit of the average particle diameter of the granular-shaped hematite particles is usually 0.075 μm, preferably 0.085 μm, more preferably 0.095 μm, and the upper limit thereof is usually 0.95 μm, preferably 0.65 μm, more preferably 0.45 μm.

(ii) In the case where the shape of the hematite particles is acicular-shaped, the lower limit of the average particle diameter (average major axis diameter) of the acicular-shaped hematite particles is usually 0.075 μm, preferably 0.085 μm, more preferably 0.095 μm, and the upper limit thereof is usually 0.95 μm, preferably 0.65 μm, more preferably 0.45 μm; and the lower limit of the aspect ratio (average major axis diameter/average minor axis diameter) of the acicular-shaped hematite particles is usually 2:1, preferably 2.5:1, more preferably 3:1, and the upper limit thereof is usually 20:1, preferably 15:1, more preferably 10:1.

(iii) In the case where the shape of the hematite particles is plate-shaped, the lower limit of the average particle diameter (average plate surface diameter) of the plate-shaped hematite particles is usually 0.075 μm, preferably 0.085 μm, more preferably 0.095 μm, and the upper limit thereof is usually 0.95 μm, preferably 0.65 μm, more preferably 0.45 μm; and the lower limit of the plate ratio (average plate surface diameter/average thickness) of the plate-shaped hematite particles is usually 2:1, preferably 2.5:1, more preferably 3:1, and the upper limit thereof is usually 50:1, preferably 45:1, more preferably 40:1.

The magnetic recording medium having the non-magnetic undercoat layer of the present invention has a coercive force value of usually 111.4 to 143.2 kA/m (1,400 to 1,800 Oe), and when the magnetic coating film is oriented by applying a magnetic field of 397.9 kA/m (5 kOe) thereto, a squareness (Br/Bm) of usually not less than 0.86, an orientation property (OR) of usually not less than 3.3, a coercive force distribution (Switching Field Distribution: SFD) of usually not more than 0.44 and an oxidation stability (ΔBm) of usually not more than 3.0%.

The point of the present invention is that by allowing cobalt to exist in the outer layer of the respective goethite particles as precursor particles of the magnetic metal particles containing iron as a main component, it is possible to obtain spindle-shaped magnetic metal particles containing iron as a main component which exhibit not only an adequate coercive force and good dispersibility and oxidation stability, but also an excellent coercive force distribution, in spite of fine particles having a less Co content.

The reason why the magnetic metal particles containing iron as a main component of the present invention can show an excellent oxidation stability, is considered by the present inventors as follows, though not clearly known. That is, since the concentration of Co is increased near the surface portion of the particles before the reduction by coating the particles with a specific amount of Co, the crystallite growth upon the reduction is accelerated, thereby advantageously enhancing the oxidation stability thereof. Further, since the structure having a high Co concentration at the surface portion of the particles can be maintained even after completion of the reduction to some extent, it is suggested that a much denser oxide coat is readily formed on the respective particles.

For this reason, the oxidation stability of the obtained magnetic metal particles containing iron as a main component can be further improved as compared to the case where whole Co forms a solid solution (i.e., Co is added only upon the goethite reaction), so that the same degree of oxidation stability is achievable by a less Co content, resulting in economically advantageous process. In addition, even with the less Co content, the oxidation stability is more excellent.

Further, it is considered that in the present invention, by controlling the specific surface area of magnetic metal particles containing iron as a main component to a low level, namely to the value satisfying the above formula showing the specific relation to the average major axis diameter, it is possible to obtain the magnetic metal particles containing iron as a main component exhibiting an adequate coercive force and a good dispersibility without deterioration in oxidation stability in spite of fine particles having a less Co content.

The spindle-shaped magnetic metal particles containing iron as a main component according to the present invention can exhibit an adequate coercive force, excellent oxidation stability, good dispersibility and excellent coercive force distribution notwithstanding the magnetic metal particles are fine particles, especially those having an average major axis diameter as small as 0.05 to 0.15 μm. Therefore, the spindle-shaped magnetic metal particles containing iron as a main component are suitably used for the production of magnetic recording media.

Since the spindle-shaped magnetic metal particles containing iron as a main component according to the present invention are fine particles and exhibit good dispersibility and excellent coercive force distribution, the magnetic recording medium produced using the magnetic metal particles can show a high image quality and a high output characteristics and, therefore, are excellent in recording reliability.

EXAMPLES

The present invention is described in more detail by Examples and Comparative Examples, but the Examples are only illustrative and, therefore, not intended to limit the scope of the present invention thereto.

Various properties were measured by the following methods.

(1) The average major axis diameter, average minor axis diameter and aspect ratio of the respective particles are expressed by averages of values measured from an electron micrograph (x30,000). The size distribution of the particles is expressed by the value obtained by dividing the standard deviation measured simultaneously with the above values, by the average major axis diameter.

(2) The Co, Al and rare earth contents were measured using an inductively coupled high-frequency plasma atomic emission spectroscope (SPS-4000 Model, manufactured by Seiko Denshi Kogyo Co., Ltd.).

(3) The specific surface area of the respective particles is expressed by the value measured by BET method using “Monosorb MS-11” (manufactured by Cantachrom Co., Ltd.).

(4) The crystallite size of the respective particles is expressed by the thickness of the crystallite in the direction perpendicular to each crystal plane of the respective particles measured by X-ray diffraction method. The crystallite size was calculated from the X-ray diffraction peak curve prepared with respect to the respective crystal planes, according to the following Scherrer's formula:

Crystallite size=Kλ/βcosθ

wherein β is a true half-width of the diffraction peak which was corrected with respect to the width of machine used (unit: radian); K is a Scherrer constant (=0.9); λ is a wavelength of X-ray used (Cu Kα-ray: 0.1542 nm); and θ is a diffraction angle (corresponding to a diffraction peak of the respective crystal planes).

(5) The ignition temperature of magnetic metal particles was measured using TG/DTA measuring device “SSC5100TG/DTA22” (manufactured by Seiko Denshi Kogyo Co., Ltd.).

(6) The magnetic properties of magnetic metal particles were measured using a vibration sample magnetometer “VSM-3S-15” (manufactured by Toei Kogyo Co., Ltd.) by applying an external magnetic field of 795.8 kA/m (10 kOe) thereto.

The respective components as shown below were charged into a 100-cc polymer bottle, and then mixed and dispersed for 8 hours using a paint shaker (manufactured by Reddevil Co., Ltd.), thereby preparing a magnetic coating composition. The thus prepared magnetic coating composition was coated on a 25 μm-thick polyethylene telephthalate film using an applicator to form a coating layer having a thickness of 50 μm thereon. The obtained coating layer was then dried in a magnetic field of 397.9 kA/m (5 kOe), thereby obtaining a magnetic coating film. The thus obtained magnetic coating film was measured to determine magnetic properties thereof.

Coating composition 3 mmφ steel balls 800 parts by weight Spindle-shaped magnetic metal 100 parts by weight particles containing iron as a main component Polyurethane resin having 20 parts by weight a sodium sulfonate group Cyclohexanone 83.3 parts by weight Methyl ethyl ketone 83.3 parts by weight Toluene 83.3 parts by weight

(7) The oxidation stability (Δσs) of the saturation magnetization (σs) of particles, and the oxidation stability (ΔBm) of saturation magnetic flux density (Bm) of the magnetic coating film were measured as follows.

The particles and the magnetic coating film were placed in a constant-temperature oven maintained at 60° C. and a relative humidity of 90%, and allowed to stand therein for one week to conduct an accelerated deterioration test. Thereafter, the saturation magnetization value of the particles and the saturation magnetic flux density of the magnetic coating film were respectively measured. The oxidation stability values Δσs and ΔBm were calculated by dividing the difference (absolute value) between the values σs and σs′ measured before and after the one-week accelerated test, and the difference (absolute value) between the values Bm and Bm′ measured before and after the one-week accelerated test, by the values σs and Bm measured before the accelerated test, respectively.

(8) The gloss of the surface of the coating film of the magnetic recording layer was measured at an angle of incidence of 45° by “glossmeter UGV-5D” (manufactured by Suga Shikenki, Co., Ltd.).

(9) The thickness of each of the non-magnetic base film, the non-magnetic undercoat layer and the magnetic recording layer constituting the magnetic recording medium was measured in the following manner by using “Digital Electronic Micrometer R351C” (manufactured by Anritsu Corp.)

The thickness (A) of a base film was first measured. Similarly, the thickness (B) (B=the sum of the thicknesses of the base film and the non-magnetic undercoat layer) of a non-magnetic substrate obtained by forming a non-magnetic undercoat layer on the base film was measured. Furthermore, the thickness (C) (C=the sum of the thicknesses of the base film, the non-magnetic undercoat layer and the magnetic recording layer) of a magnetic recording medium obtained by forming a magnetic recording layer on the non-magnetic substrata was measured. The thickness of the non-magnetic undercoat layer is expressed by (B)−(A), and the thickness of the magnetic recording layer is expressed by (C)−(B).

Example 1

<Production of Granulated Product of Spindle-shaped Goethite Particles>

30 liters of a mixed aqueous alkali solution containing sodium carbonate and aqueous sodium hydroxide solution in amounts of 25 mol and 19 mol, respectively (the concentration of sodium hydroxide is equivalent to 27.5 mol % (calculated as normality) based on mixed alkali) was charged into a bubble tower. The inside temperature of the tower was adjusted to 47° C. while passing a nitrogen gas therethrough at a superficial velocity of 2.20 cm/s. Then, 20 liters of an aqueous ferrous sulfate solution containing 20 mol of Fe²⁺ (the concentration of the mixed aqueous alkali solution is 1.725 equivalents (calculated as normality) based on the ferrous sulfate) was charged into the bubble tower and the contents of the bubble tower were aged therein for 45 minutes. Thereafter, 4 liters of an aqueous cobalt sulfate solution containing 0.96 mol of Co²⁺ (equivalent to 4.8 atm % (calculated as Co) based on whole Fe) was added to the bubble tower and the contents of the bubble tower were further aged for 4 hours and 15 minutes (percentage of time required for Co addition based on whole aging time: 15%). After aging, air was passed through the bubble tower at a superficial velocity of 2.50 cm/s to conduct the oxidation reaction until the oxidation percentage of Fe²⁺ reached 40%, thereby producing goethite seed crystal particles.

Then, one liter of an aqueous aluminum sulfate solution containing 1.6 mol of Al³⁺ (equivalent to 8.0 atm % (calculated as Al) based on whole Fe) was added at a feed rate of not more than 3 ml/s to conduct the oxidation reaction, and the reaction mixture was washed with water using a filter press until the electric conductivity reached 60 μS/cm, thereby obtaining a press cake.

A part of the obtained press cake was dried and pulverized by ordinary methods, thereby obtaining spindle-shaped goethite particles. The obtained goethite particles were of a spindle shape, and had an average major axial diameter of 0.153 μm, a standard deviation σ of 0.0300 μm, a size distribution (standard deviation/major axial diameter) of 0.196, an average minor axial diameter of 0.0244 μm, an aspect ratio of 6.3:1 and a BET specific surface area of 169.3 m²/g. The obtained goethite particles contained no dendritic particles, and had a crystallite size D₀₂₀ of 194 Å, a crystallite size D₁₁₀ of 109 Å and a crystallite size ratio D₀₂₀/D₁₁₀ of 1.78.

Further, it was confirmed that the obtained goethite particles had a Co content of 4.8 atm % based on whole Fe and an Al content of 8.0 atm % based on whole Fe, and Al was contained only in the surface layer portion.

<Second Step: Production of Starting Particles>

Then, a press cake containing 1,000 g of the thus obtained spindle-shaped goethite particles (9.22 mol calculated as Fe) was sufficiently dispersed in 40 liters of water. The resultant dispersion was mixed with 2 liters of an aqueous neodymium nitrate solution containing 121.2 g of neodymium nitrate hexahydrate (corresponding to 3.0 atm % (calculated as Nd) based on whole Fe contained in the goethite particles) and 2 liters of an aqueous cobalt sulfate solution containing 51.8 g of cobalt sulfate heptahydrate (corresponding to 2.0 atm % (calculated as Co) based on whole Fe, and 41.7% based on Co contained in the spindle-shaped goethite particles) while stirring. The pH value of the resultant mixture was adjusted to 9.5 by adding a 25.0 wt. % sodium carbonate aqueous solution as a precipitating agent thereto. After the mixture was washed by a filter press, the obtained press cake was extrusion-molded though a mold plate having an orifice diameter of 4 mm using a compression-molding machine, and then dried at 120° C., thereby obtaining a granulated product of starting particles.

The goethite particles obtained by pulverizing the molded.product had a Co content of 6.8 atm % based on whole Fe; an Al content of 8.0 atm % based on whole Fe; and a Nd content of 3.0 atm % based on whole Fe. In addition, it was confirmed that Al was contained only in the goethite layer portion of each goethite particle, and Nd was contained only in the surface layer portion thereof.

The spindle-shaped goethite particles coated with the cobalt compounds and the neodymium compound were heat-dehydrated in air at 720 to obtain spindle-shaped hematite particles having an outer layer composed of the cobalt compounds and the neodymium compound, such that the ratio of the crystallite size D₁₀₄ of the obtained spindle-shaped hematite particles to the crystallite size D₁₁₀ of the spindle-shaped goethite particles [crystallite size ratio: D₁₀₄(hematite)/D₁₁₀(goethite)] was in the range of 1.0 to 1.3.

The obtained spindle-shaped hematite particles were of a spindle shape, and had an average major axial diameter of 0.139 mm, a standard deviation s of 0.0301 μm, a size distribution (standard deviation/average major axial diameter) of 0.217, an average minor axial diameter of 0.0198 μm, an aspect ratio of 7.0:1 and a BET specific surface area of 45.1 m²/g. In addition, it was confirmed that the Co content of the hematite particles was 6.8 atm % based on whole Fe; the Al content thereof was 8.0 atm % based on whole Fe; and the Nd content thereof was 3.0 atm % based on whole Fe. Further, the obtained spindle-shaped hematite particles had a crystallite size D₁₀₄ of 122 Å and a crystallite size ratio: D₁₀₄(hematite)/D₁₁₀(goethite) of 1.12; and a crystallite size D₁₁₀ of 266 Å and a crystallite size ratio: D₁₁₀(hematite)/D₁₀₄(hematite) of 2.18.

<Fourth Step: Production of Spindle-shaped Magnetic Metal Particles Containing Iron as a Main Component>

Then, the obtained spindle-shaped hematite particles having the outer layer composed of the cobalt compounds and the neodymium compound were charged into a reducing apparatus to form a fixed-bed having a height of 7 cm. The spindle-shaped hematite particles were heated to 470° C. at a temperature-rising rate of 20° C./minute while passing a hydrogen (H₂) gas through the reducing apparatus at a superficial velocity of 70 cm/s at 470° C., and successively heat-reduced. Thereafter, the hydrogen gas was replaced with a nitrogen gas, the particles were cooled to 70° C., and then the oxygen partial pressure in the reducing apparatus was gradually increased by passing water vapor therethrough until the oxygen content therein reached the same content as in air, thereby forming a stable oxide film on the surface of the respective particles.

A part of the thus obtained spindle-shaped magnetic metal particles was sampled from the lower portion (corresponding to a height of not more than 2 cm) and upper portion (corresponding to a height of not less than 5 cm) of the fixed-bed, respectively, and measured separately from the remaining part of the fixed-bed to determine magnetic properties and crystallite size thereof.

As a result, it was confirmed that the obtained magnetic metal particles containing iron as a main component had an average major axis diameter of 0.125 μm, a standard deviation σ of 0.0288 μm, a size distribution (standard deviation/average major axis diameter) of 0.230, an average minor axis diameter of 0.0190 μm, an aspect ratio of 6.6:1, a BET specific surface area of 42.7 m²/g and a crystallite size of 153 Å, and further the magnetic metal particles had a spindle shape and a uniform particle size, and contained a less amount of dendritic particles. In addition, it was confirmed that the Co content of the magnetic metal particles was 6.8 atm % based on whole Fe; the Al content thereof was 8.0 atm % based on whole Fe; and the Nd content thereof was 3.0 atm % based on whole Fe. As to the magnetic properties of the spindle-shaped magnetic metal particles, it was confirmed that the coercive force thereof was 136.9 kA/m (1,720 Oe); the saturation magnetization σs thereof was 126.4 Am²/kg (126.4 emu/g); the squareness (σr/σs) thereof was 0.491; the oxidation stability Δσs of saturation magnetization thereof was 3.3% as an absolute value (measured value: −3.3%); and the ignition temperature thereof was 150° C.

Meanwhile, a part of the thus obtained particles was sampled from the lower portion (corresponding to a height of not more than 2 cm) and upper portion (corresponding to a height of not less than 5 cm) of the fixed-bed, respectively, and measured separately from the remaining part of the fixed-bed to determine magnetic properties and crystallite size thereof. As a result, it was confirmed that the coercive force Hc thereof was 137.5 kA/m (1,728 Oe); the saturation magnetization σs thereof was 125.9 Am²/kg (125.9 emu/g); the squareness (σr/σs) thereof was 0.492; and the X-ray-measured crystallite size D₁₁₀ thereof was 151 Å. As to the magnetic properties of the spindle-shaped magnetic metal particles sampled from the upper portion of the fixed-bed, it was confirmed that the coercive force Hc thereof was 136.12 kA/m (1,711 Oe); the saturation magnetization σs thereof was 126.8 Am²/kg (126.8 emu/g); the squareness (σr/σs) thereof was 0.490; and the X-ray-measured crystallite size D₁₁₀ thereof was 154 Å.

Further, as to sheet magnetic characteristics, it was confirmed that the sheet coercive force Hc was 136.4 kA/m (1,714 Oe); the sheet squareness (Br/Bm) was 0.851; the sheet orientation property (OR) was 3.20; the sheet SFD was 0.490; and ΔBm was 2.7% (measured value: −2.7%).

Examples 2 to 5 and Comparative Examples 1 to 4 Goethite Particles 1 to 5

<First Step: Production of Goethite Particles>

The same procedure as defined in Example 1 was conducted except that production conditions of goethite particles, i.e., production reaction conditions of goethite seed crystal particles and growth reaction conditions, were varied as shown in Table 1, thereby obtaining spindle-shaped goethite particles. Various properties of the obtained goethite particles are shown in Table 2. Meanwhile, in Table 1, the alkali ratio was calculated from the following formula:

Alkali ratio=(½ alkali hydroxide)/(whole alkali)

wherein the whole alkali is a sum of ½ alkali hydroxide and alkali carbonate.

In addition, the equivalent ratio was calculated from the following formula:

Equivalent ratio=(whole alkali)/(Fe²⁺)

wherein the whole alkali is a sum of ½ alkali hydroxide and alkali carbonate.

<Second Step: Production of Starting Particles>

The same procedure as defined in Example 1 was conducted except that the goethite particles 1 to 5 produced in the first step were used, and kind and amount of rare earth element and amount of Co added were changed variously, thereby obtaining starting particles. Production conditions used thereupon are shown in Table 3.

<Third Step: Production of Hematite Particles>

The same procedure as defined in Example 1 was conducted except that the starting particles 1 to 8 produced in the second step were used, heat-dehydrating temperature and subsequent heat-treating temperature were changed variously, thereby obtaining hematite particles. Production conditions used thereupon are shown in Table 3, and various properties of the obtained hematite particles are shown in Table 4.

<Fourth Step: Production of Spindle-shaped Magnetic Metal Particles>

The same procedure as defined in Example 1 was conducted except that the hematite particles 1 to 8 obtained in the above third step were used, and height of fixed-bed, kind of gas used upon heating, superficial velocity of reducing gas, temperature-rising rate and heat-reducing temperature was changed variously, thereby producing magnetic metal particles. Production conditions and various properties of the obtained spindle-shaped magnetic metal particles are shown in Tables 5 and 6; various properties of the magnetic metal particles sampled from the upper and lower portions of the fixed-bed are shown in Table 7; and

various properties of the sheet produced using the obtained magnetic metal particles are shown in Table 8.

Example 6

<Production of Magnetic Recording Medium>

100 parts by weight of the spindle-shaped magnetic metal particles obtained in Example 3, 10.0 parts by weight of a vinyl chloride-vinyl acetate copolymer resin (tradename: MR-110, produced by Nippon Zeon Co., Ltd.), 23.3 parts by weight of cyclohexanone, 10.0 parts by weight of methyl ethyl ketone, 1.0 part by weight of carbon black particles (produced by Mitsubishi Chemical Corp., average particle size: 26 nm; BET specific surface area: 130 m²/g) and 7.0 parts by weight of alumina particles “AKP-30” (tradename, produced by Sumitomo Kagaku Co., Ltd., average particle size: 0.4 μm) were kneaded together for 20 minutes using a kneader. The obtained kneaded material was diluted by adding 79.6 parts by weight of toluene, 110.2 parts by weight of methyl ethyl ketone and 17.8 parts by weight of cyclohexanone thereto, and then the resultant mixture was mixed and dispersed for 3 hours by a sand grinder, thereby obtaining a dispersion.

The obtained dispersion was mixed with 33.3 parts by weight of a solution prepared by dissolving 10.0 parts by weight (solid content) of a polyurethane resin (tradename: E-900, produced by Takeda Yakuhin Kogyo Co., Ltd.) in a mixed solvent containing methyl ethyl ketone and toluene at a mixing ratio of 1:1, and the resultant mixture was mixed and dispersed for 30 minutes by a sand grinder. Thereafter, the obtained dispersion was passed through a filter having a mesh size of 1 μm. The obtained filter cake was mixed under stirring with 12.1 parts by weight of a solution prepared by dissolving 1.0 part by weight of myristic acid and 3.0 parts by weight of butyl stearate in a mixed solvent containing methyl ethyl ketone, toluene and cyclohexanone at a mixing ratio (weight) of 5:3:2, and with 15.2 parts by weight of a solution prepared by dissolving 5.0 parts by weight of trifunctional low molecular weight polyisocyanate (tradename: E-31, produced by Takeda Yakuhin Kogyo Co., Ltd.) in a mixed solvent containing methyl ethyl ketone, toluene and cyclohexanone at a mixing ratio (weight) of 5:3:2, thereby producing a magnetic coating composition.

The obtained magnetic coating composition contained the following components:

Spindle-shaped magnetic metal 100 weight parts particles Vinyl chloride-vinyl acetate 10 weight parts copolymer resin Polyurethane resin 10 weight parts Alumina particles 7.0 weight parts Carbon black fine particles 1.0 weight part Myristic acid 1.0 weight part Butyl stearate 3.0 weight parts Trifunctional low molecular 5.0 weight parts weight polyisocyanate Cyclohexanone 56.6 weight parts Methyl ethyl ketone 141.5 weight parts Toluene 85.4 weight parts

The obtained magnetic coating composition had a viscosity of 5,650 cP.

The thus obtained magnetic coating composition was passed through a filter having a mesh size of 1 μm. Thereafter, the magnetic coating composition was coated on a 12 μm-thick polyester base film using a slit coater having a gap width of 45 μm and then dried, thereby forming a magnetic layer on the base film. The surface of the obtained magnetic recording layer was calendered and smoothened by an ordinary method, and then the film was cut into a width of ½ inch (1.27 cm). The obtained tape was allowed to stand in a curing oven maintained at 60° C., for 24 hours to sufficiently cure the magnetic recording layer therein, thereby producing a magnetic tape. The obtained coating layer had a thickness of 3.5 μm.

With respect to magnetic properties of the obtained magnetic tape, the coercive force value thereof was 143.5 kA/m (1803 Oe); the gloss thereof was 231%; the squareness (Br/Bm) thereof was 0.877; the sheet orientation property (OR) was 3.45; the sheet SFD was 0.421; and ΔBm was 2.2% as an absolute value (measured value: −2.2%).

Example 7

<Production of Non-magnetic Undercoat Layer>

12 g of non-magnetic particles (kind: hematite particles; particle shape: spindle-shaped; average major axial diameter: 0.187 μm; average minor axial diameter: 0.0240 μm; aspect ratio: 7.8:1; geometrical standard deviation value: 1.33; BET specific surface area value: 43.3 m²/g; volume resistivity value: 8.6×10⁸ Ω·cm; blackness (L* value): 32.6) were mixed with a binder resin solution (containing 30% by weight of vinyl chloride-vinyl acetate copolymer resin having a sodium sulfonate group and 70% by weight of cyclohexanone) and cyclohexanone, thereby obtaining a mixture (solid content: 72%). The obtained mixture was further kneaded for 30 minutes using a plastomill, thereby obtaining a kneaded material.

The thus obtained kneaded material was added to a 140 ml glass bottle together with 95 g of 1.5 mmφ glass beads, an additional amount of a binder resin solution (containing 30% by weight of polyurethane resin having a sodium sulfonate group and 70% by weight of a mixed solvent of methyl ethyl ketone and toluene (1:1)), cyclohexanone, methyl ethyl ketone and toluene. The resultant mixture was mixed and dispersed for 6 hours by a paint shaker, thereby obtaining a coating composition. Thereafter, a lubricant was added to the obtained coating composition, and the mixture was mixed and dispersed for 15 minutes by a paint shaker.

The composition of the obtained non-magnetic coating composition was as follows:

Non-magnetic particles 1 100 parts by weight Vinyl chloride-vinyl acetate 10 parts by weight copolymer resin having a sodium sulfonate group Polyurethane resin having 10 parts by weight a sodium sulfonate group Lubricant (myristic acid: 2 parts by weight butyl stearate = 1:1) Cyclohexanone 56.9 parts by weight Methyl ethyl ketone 142.3 parts by weight Toluene 85.4 parts by weight

The obtained non-magnetic coating composition had a viscosity of 310 cP.

Next, the non-magnetic coating composition was coated on a 12 μm-thick polyethylene terephthalate film using an applicator so as to form thereon a 55 μm-thick coating layer, and then dried, thereby producing a non-magnetic undercoat layer.

The thus obtained non-magnetic undercoat layer had a thickness of 3.4 μm, and exhibited a gloss of 193%, a surface roughness Ra of 8.2 nm, a Young's modulus (relative value) of 123, a linear absorption of 1.01 μm⁻¹ and a surface electrical resistivity value of 1.1×10¹⁴ Ω·cm.

<Production of Magnetic Recording Medium>

100 parts by weight of the spindle-shaped magnetic metal particles obtained in Example 3, 10.0 parts by weight of a vinyl chloride-vinyl acetate copolymer resin (tradename: MR-110, produced by Nippon Zeon Co., Ltd.), 23.3 parts by weight of cyclohexanone, 10.0 parts by weight of methyl ethyl ketone, 1.0 part by weight of carbon black particles (produced by Mitsubishi Chemical Corp., average particle size: 26 nm; BET specific surface area: 130 m²/g) and 7.0 parts by weight of alumina particles “AKP-30” (tradename, produced by Sumitomo Kagaku Co., Ltd., average particle size: 0.4 μm) were kneaded together for 20 minutes using a kneader. The obtained kneaded material was diluted by adding 79.6 parts by weight of toluene, 110.2 parts by weight of methyl ethyl ketone and 17.8 parts by weight of cyclohexanone thereto, and then the resultant mixture was mixed and dispersed for 3 hours by a sand grinder, thereby obtaining a dispersion.

The obtained dispersion was mixed with 33.3 parts by weight of a solution prepared by dissolving 10.0 parts by weight (solid content) of a polyurethane resin (tradename: E-900, produced by Takeda Yakuhin Kogyo Co., Ltd.) in a mixed solvent containing methyl ethyl ketone and toluene at a mixing ratio of 1:1, and the resultant mixture was mixed and dispersed for 30 minutes by a sand grinder. Thereafter, the obtained dispersion was passed through a filter having a mesh size of 1 μm. The obtained filter cake was mixed under stirring with 12.1 parts by weight of a solution prepared by dissolving 1.0 part by weight of myristic acid and 3.0 parts by weight of butyl stearate in a mixed solvent containing methyl ethyl ketone, toluene and cyclohexanone at a mixing ratio (weight) of 5:3:2, and with 15.2 parts by weight of a solution prepared by dissolving 5.0 parts by weight of trifunctional low molecular weight polyisocyanate (tradename: E-31, produced by Takeda Yakuhin Kogyo Co., Ltd.) in a mixed solvent containing methyl ethyl ketone, toluene and cyclohexanone at a mixing ratio (weight) of 5:3:2, thereby producing a magnetic coating composition.

The obtained magnetic coating composition contained the following components:

Spindle-shaped magnetic metal 100 weight parts particles Vinyl chloride-vinyl acetate 10 weight parts copolymer resin Polyurethane resin 10 weight parts Alumina particles 7.0 weight parts Carbon blackfine particles 1.0 weight part Myristic acid 1.0 weight part Butyl stearate 3.0 weight parts Trifunctional low molecular 5.0 weight parts weight polyisocyanate Cyclohexanone 56.6 weight parts Methyl ethyl ketone 141.5 weight parts Toluene 85.4 weight parts

The obtained magnetic coating composition had a viscosity of 5,650 cP.

The thus obtained magnetic coating composition was passed through a filter having a mesh size of 1 μm. Thereafter, the magnetic coating composition was coated on the obtained non-magnetic undercoat layer using a slit coater having a gap width of 45 μm and then dried, thereby forming a magnetic layer on the base film. The surface of the obtained magnetic recording layer was calendered and smoothed by an ordinary method, and then the film was cut into a width of ½ inch (1.27 cm). The obtained tape was allowed to stand in a curing oven maintained at 60° C., for 24 hours to sufficiently cure the magnetic recording layer therein, thereby producing a magnetic tape. The obtained coating layer had a thickness of 3.5 μm.

With respect to magnetic properties of the obtained magnetic tape, the coercive force value thereof was 143.1 kA/m (1798 Oe); the gloss thereof was 242%; the squareness (Br/Bm) thereof was 0.879; the sheet orientation property (OR) was 3.47; the sheet SFD was 0.419; and ΔBm was 2.4% as an absolute value (measured value: −2.4%).

TABLE 1 Production of spindle-shaped goethite particles Production reaction of goethite seed crystal particles Mixed aqueous alkali solution Aqueous alkali Aqueous alkali carbonate hydroxide solution solution Amount Amount Alkali Goethite used used ratio¹⁾ particles Kind (mol) Kind (mol) (mol %) Goethite Na₂CO₃ 25 NaOH 19 27.5 particles 1 Goethite Na₂CO₃ 25 NaOH 19 27.5 particles 2 Goethite Na₂CO₃ 25 NaOH 19 27.5 particles 3 Goethite Na₂CO₃ 25 NaOH 19 27.5 particles 4 Goethite Na₂CO₃ 25 NaOH 19 27.5 particles 5 ¹⁾Alkali ratio = (½•alkali hydroxide)/(whole alkali) wherein whole alkali is a sum of ½•alkali hydroxide and alkali carbonate Production of spindle-shaped goethite particles Production reaction of goethite seed crystal particles Aqueous ferrous salt solution Goethite Amount used Equivalent particles Kind (mol) ratio²⁾ Goethite FeSO₄ 20 1.725 particles 1 Goethite FeSO₄ 20 1.725 particles 2 Goethite FeSO₄ 20 1.725 particles 3 Goethite FeSO₄ 20 1.725 particles 4 Goethite FeSO₄ 20 1.725 particles 5 ²⁾Equivalent ratio = (whole alkali)/(Fe²⁺) wherein whole alkali is a sum of ½•alkali hydroxide and alkali carbonate Production of spindle-shaped goethite particles Production reaction of goethite seed crystal particles Aging Superficial velocity of Goethite Temperature Time nitrogen passed particles (° C.) (hr) (cm/s) Goethite 48 5 2.30 particles 1 Goethite 46 5 2.50 particles 2 Goethite 46 5 2.40 particles 3 Goethite 47 5 2.50 particles 4 Goethite 47 5 2.20 particles 5 Production of spindle-shaped goethite particles Production reaction of goethite seed crystal particles Cobalt compound Addition time after Amount initiation (Co addition added of time)/(whole Goethite (Co/Fe) aging aging time) particles Kind (atom %) (hr) (%) Goethite CoSO₄ 4.9 0.50 10 particles 1 Goethite CoSO₄ 4.5 0.75 15 particles 2 Goethite CoSO₄ 4.8 1.25 25 particles 3 Goethite CoSO₄ 4.8 1.75 35 particles 4 Goethite CoSO₄ 10.0 2.00 40 particles 5 Production of spindle-shaped goethite particles Production reaction of goethite seed crystal particles Goethite Superficial velocity particles of airpassed (cm/s) Temperature (° C.) Goethite 2.60 48 particles 1 Goethite 2.80 46 particles 2 Goethite 3.00 46 particles 3 Goethite 3.00 47 particles 4 Goethite 2.00 47 particles 5 Production of spindle-shaped goethite particles Growth reaction of seed crystal particles Aluminum compound Addition Amount time Superficial added (oxidation velocity of Goethite (Al/Fe) percentage air passed particles Kind (atom %) of Fe²⁺) (%) (cm/s) Goethite Aluminum 8.0 40 2.60 particles 1 sulfate Goethite Aluminum 8.0 40 2.80 particles 2 sulfate Goethite Aluminum 7.5 40 3.00 particles 3 sulfate Goethite Aluminum 9.0 40 3.00 particles 4 sulfate Goethite Aluminum 7.0 40 3.30 particles 5 sulfate

TABLE 2 Properties of spindle-shaped goethite particles Average major Standard Goethite axis diameter deviation (σ) particles Shape (L) (μm) (μm) Goethite Spindle- 0.149 0.0277 particles 1 shaped Goethite Spindle- 0.138 0.0235 particles 2 shaped Goethite Spindle- 0.130 0.0221 particles 3 shaped Goethite Spindle- 0.118 0.0196 particles 4 shaped Goethite Spindle- 0.134 0.0264 particles 5 shaped Properties of spindle-shaped goethite particles BET Average specific Size minor axis surface Goethite distribution diameter Aspect area particles (σ/L) (μm) ratio (m²/g) Goethite 0.186 0.0254 5.9:1 154.5 particles 1 Goethite 0.170 0.0242 5.7:1 162.1 particles 2 Goethite 0.170 0.0236 5.5:1 171.8 particles 3 Goethite 0.166 0.0215 5.5:1 166.8 particles 4 Goethite 0.197 0.0172 7.8:1 169.5 particles 5 Properties of spindle-shaped goethite particles Composition of whole particles Co content Al content Goethite (Co/Fe) (Al/Fe) particles (atom %) (atom %) Goethite 4.9 8.0 particles 1 Goethite 4.5 8.0 particles 2 Goethite 4.8 7.5 particles 3 Goethite 4.8 9.0 particles 4 Goethite 10.0 7.0 particles 5 Properties of spindle-shaped goethite particles Crystallite size Crystallite size Goethite D₀₂₀ D₁₁₀ ratio particles (Å) (Å) D₀₂₀/D₁₁₀ Goethite 188 111 1.69 particles 1 Goethite 185 106 1.75 particles 2 Goethite 184 103 1.79 particles 3 Goethite 179 103 1.74 particles 4 Goethite 170 103 1.65 particles 5

TABLE 3 Production conditions of starting particles surface additives Goethite Kind of cobalt compound Hematite particles contained in treating particles used agent Hematite Goethite Cobalt sulfate particles 1 particles 1 Hematite Goethite Cobalt sulfate particles 2 particles 2 Hematite Goethite Cobalt sulfate particles 3 particles 3 Hematite Goethite Cobalt sulfate particles 4 particles 4 Hematite Goethite Cobalt sulfate particles 5 particles 1 Hematite Goethite Cobalt sulfate particles 6 particles 2 Hematite Goethite Cobalt sulfate particles 7 particles 5 Hematite Goethite Cobalt sulfate particles 8 particles 3 Production conditions of starting particles surface additives Co ratio (Co coating amount)/ Amount added (Co content in Hematite (Co/Fe) goethite particles) particles (atom %) (%) Hematite 2.0 40.8 particles 1 Hematite 5.0 111.1 particles 2 Hematite 5.5 114.6 particles 3 Hematite 8.0 166.7 particles 4 Hematite 10.0 204.1 particles 5 Hematite 0.5 11.1 particles 6 Hematite 0.0 — particles 7 Hematite 7.0 145.8 particles 8 Production conditions of starting particles Anti-sintering treatment Kind of rare earth Amount added Hematite compound contained in (Re/Fe) particles anti-sintering agent (atom %) Hematite Neodymium nitrate 3.5 particles 1 Hematite Yttrium nitrate 4.0 particles 2 Hematite Yttrium nitrate 4.2 particles 3 Hematite Neodymium nitrate 4.8 particles 4 Hematite Neodymium nitrate 3.5 particles 5 Hematite Yttrium nitrate 4.0 particles 6 Hematite Neodymium nitrate 4.0 particles 7 Hematite — 0.0 particles 8 Production conditions of spindle-shaped hematite particles Hematite Heating particles temperature (° C.) Atmosphere Hematite 740 Air particles 1 Hematite 730 Air particles 2 Hematite 700 Air particles 3 Hematite 710 Air particles 4 Hematite 740 Air particles 5 Hematite 730 Air particles 6 Hematite 700 Air particles 7 Hematite 700 Air particles 8

TABLE 4 Properties of spindle-shaped hematite particles Standard Average major deviation Size Hematite axis diameter (σ) distribution particles (L) (μm) (μm) (σ/L) Hematite 0.133 0.0269 0.202 particles 1 Hematite 0.129 0.0222 0.172 particles 2 Hematite 0.120 0.0201 0.168 particles 3 Hematite 0.101 0.0176 0.174 particles 4 Hematite 0.130 0.0298 0.229 particles 5 Hematite 0.131 0.0215 0.164 particles 6 Hematite 0.124 0.0230 0.185 particles 7 Hematite 0.118 0.0277 0.235 particles 8 Properties of spindle-shaped hematite particles Average minor BET specific Hematite axis diameter Aspect surface area particles (μm) ratio (m²/g) Hematite 0.0204 6.5:1 43.0 particles 1 Hematite 0.0205 6.3:1 41.9 particles 2 Hematite 0.0197 6.1:1 45.6 particles 3 Hematite 0.0168 6.0:1 51.9 particles 4 Hematite 0.0210 6.2:1 34.1 particles 5 Hematite 0.0205 6.4:1 42.3 particles 6 Hematite 0.0166 7.5:1 62.0 particles 7 Hematite 0.0203 5.8:1 31.6 particles 8 Properties of spindle-shaped hematite particles Composition of whole particles Rare earth Co content Al content content Hematite (Co/Fe) (Al/Fe) (Re/Fe) particles (atom %) (atom %) (atom %) Hematite 6.9 8.0 3.5 particles 1 Hematite 9.5 8.0 4.0 particles 2 Hematite 10.3 7.5 4.2 particles 3 Hematite 12.8 9.0 4.8 particles 4 Hematite 14.9 8.0 3.5 particles 5 Hematite 5.0 8.0 4.0 particles 6 Hematite 10.0 7.0 4.0 particles 7 Hematite 11.8 7.5 0.0 particles 8 Properties of spindle-shaped hematite particles Crystallite size Hematite D₁₀₄ D₁₁₀ particles (Å) (Å) Hematite 124 269 particles 1 Hematite 115 249 particles 2 Hematite 118 240 particles 3 Hematite 110 229 particles 4 Hematite 145 303 particles 5 Hematite 114 245 particles 6 Hematite 130 260 particles 7 Hematite 148 305 particles 8 Properties of spindle-shaped hematite particles Goethite Crystallite crystallite size ratio of Crystallite size hematite to Hematite size ratio (D₁₁₀ (g)) goethite particles (D₁₁₀/D₁₀₄) (Å) (D₁₀₄/D₁₁₀ (g)) Hematite 2.17 111 1.12 particles 1 Hematite 2.17 106 1.08 particles 2 Hematite 2.03 103 1.15 particles 3 Hematite 2.08 103 1.07 particles 4 Hematite 2.09 111 1.31 particles 5 Hematite 2.15 106 1.08 particles 6 Hematite 2.00 1.03 1.26 particles 7 Hematite 2.06 103 1.44 particles 8

TABLE 5 Examples and Comparative Examples Kind of hematite particles used Example 2 Hematite particles 1 Example 3 Hematite particles 2 Example 4 Hematite particles 3 Example 5 Hematite particles 4 Comparative Hematite particles 5 Example 1 Comparative Hematite particles 6 Example 2 Comparative Hematite particles 7 Example 3 Comparative Hematite particles 8 Example 4 Examples Conditions of reduction and Height of Comparative fixed bed Kind of Kind of Examples (cm) heating gas reducing gas Example 2 8 H₂ H₂ Example 3 6 H₂ H₂ Example 4 5 H₂ H₂ Example 5 7 H₂ H₂ Comparative 8 H₂ H₂ Example 1 Comparative 6 H₂ H₂ Example 2 Comparative 5 H₂ H₂ Example 3 Comparative 5 H₂ H₂ Example 4 Examples Conditions of reduction and Superficial Temperature Reducing Comparative velocity rise rate temperature Examples (cm/s) (° C./min.) (° C.) Example 2 80 30 460 Example 3 100 40 480 Example 4 120 25 450 Example 5 120 25 440 Comparative 80 30 460 Example 1 Comparative 100 40 480 Example 2 Comparative 70 20 500 Example 3 Comparative 120 25 420 Example 4

TABLE 6 Properties of magnetic metal particles Examples containing iron as a main component and Average major Standard Size Comparative axis diameter deviation (σ) distribution Examples (L) (μ) (μm) (σ/L) Example 2 0.120 0.0265 0.221 Example 3 0.113 0.0221 0.196 Example 4 0.095 0.0198 0.208 Example 5 0.085 0.0188 0.221 Comparative 0.114 0.0344 0.302 Example 1 Comparative 0.115 0.0219 0.190 Example 2 Comparative 0.110 0.0180 0.164 Example 3 Comparative 0.091 0.0292 0.321 Example 4 Properties of magnetic metal particles Examples containing iron as a main component and Average minor BET specific Comparative axis diameter Aspect surface area Examples (μm) ratio (S) (m²/g) Example 2 0.0194 6.2:1 42.2 Example 3 0.0192 5.3:1 41.0 Example 4 0.0170 5.6:1 43.8 Example 5 0.0160 5.3:1 43.9 Comparative 0.0190 6.0:1 34.9 Example 1 Comparative 0.0189 6.1:1 42.0 Example 2 Comparative 0.0161 6.8:1 44.1 Example 3 Comparative 0.0186 4.9:1 29.1 Example 4 Properties of magnetic metal particles Examples containing iron as main component and Crystallite size Comparative General formula: D₁₁₀ Examples −160 × L + 65 (Å) Example 2 45.80 154 Example 3 46.92 157 Example 4 49.80 155 Example 5 51.40 151 Comparative 46.76 169 Example 1 Comparative 46.60 154 Example 2 Comparative 47.40 141 Example 3 Comparative 50.44 178 Example 4 Properties of magnetic metal particles containing iron as main component Examples Rare earth and Co content Al content content Comparative (Co/Fe) (Al/Fe) (Re/Fe) Examples (atom %) (atom %) (atom %) Example 2 6.9 8.0 3.5 Example 3 9.5 8.0 4.0 Example 4 10.3 7.5 4.2 Example 5 12.8 9.0 4.8 Comparative 14.9 8.0 3.5 Example 1 Comparative 5.0 8.0 4.0 Example 2 Comparative 10.0 7.0 4.0 Example 3 Comparative 11.8 7.5 0.0 Example 4

TABLE 7 Properties of magnetic metal particles containing iron as main component Magnetic properties of lower portion of fixed bed (portion of hot more than 2 cm Examples from bottom) and Saturation Comparative Coercive force magnetization Examples (kA/m) (Oe) (Am²/kg) (emu/g) Example 2 137.7 1,730 127.9 127.9 Example 3 142.3 1,788 128.1 128.1 Example 4 146.8 1,845 129.4 129.4 Example 5 154.4 1,940 134.1 134.1 Comparative 128.0 1,609 131.5 131.5 Example 1 Comparative 138.1 1,735 122.7 122.7 Example 2 Comparative 154.8 1,945 125.3 125.3 Example 3 Comparative 105.7 1,328 128.9 128.9 Example 4 Properties of magnetic metal particles containing iron as main component Magnetic properties of lower portion of fixed bed (portion of not more than 2 cm Examples from bottom) and Crystallite size Comparative Squareness (σr/σs) D₁₁₀ Examples (−) (Å) Example 2 0.497 152 Example 3 0.495 155 Example 4 0.497 153 Example 5 0.509 150 Comparative 0.484 167 Example 1 Comparative 0.492 152 Example 2 Comparative 0.515 138 Example 3 Comparative 0.475 175 Example 4 Properties of magnetic metal particles containing iron as main component Magnetic properties of upper portion of fixed bed (portion of not more than 2 cm Examples from top) and Saturation Comparative Coercive force magnetization Examples (kA/m) (Oe) (Am²/kg) (emu/g) Example 2 136.6 1,716 129.0 129.0 Example 3 140.8 1,769 128.8 128.8 Example 4 145.3 1,826 130.6 130.6 Example 5 152.9 1,922 136.0 136.0 Comparative 125.6 1,578 134.6 134.6 Example 1 Comparative 136.5 1,715 124.5 124.5 Example 2 Comparative 153.1 1,924 129.1 129.1 Example 3 Comparative 100.1 1,258 135.1 135.1 Example 4 Properties of magnetic metal particles containing iron as main component Magnetic properties of upper portion of fixed bed (portion of not more than 2 cm Examples from top) and Crystallite size Comparative Squareness D₁₁₀ Examples (−) (Å) Example 2 0.494 156 Example 3 0.493 158 Example 4 0.494 157 Example 5 0.506 154 Comparative 0.478 173 Example 1 Comparative 0.489 156 Example 2 Comparative 0.511 146 Example 3 Comparative 0.468 186 Example 4 Properties of magnetic metal particles containing iron as main component Difference in magnetic properties between lower and upper portions of Examples fixed bed (Δ) and Saturation Comparative Coercive force magnetization Examples (kA/m) (Oe) (Am²/kg) (emu/g) Example 2 1.1 14 1.1 1.1 Example 3 1.5 19 0.7 0.7 Example 4 1.5 19 1.2 1.2 Example 5 1.5 18 1.9 1.9 Comparative 2.4 31 3.1 3.1 Example 1 Comparative 1.6 20 1.8 1.8 Example 2 Comparative 1.7 21 3.8 3.8 Example 3 Comparative 5.6 70 6.2 6.2 Example 4 Properties of magnetic metal particles containing iron as main component Difference in magnetic properties between lower and upper portions of fixed bed Examples (Δ) and Crystallite size Comparative Squareness D₁₁₀ Examples (−) (Å) Example 2 0.003 4 Example 3 0.002 3 Example 4 0.003 4 Example 5 0.003 4 Comparative 0.006 6 Example 1 Comparative 0.003 4 Example 2 Comparative 0.004 8 Example 3 Comparative 0.007 11 Example 4

TABLE 8 Properties of magnetic metal particles Examples containing iron as main component and Coercive force Saturation Comparative (Hc) magnetization (σs) Examples (kA/m) (Oe) (Am²/kg) (emu/g) Example 2 137.2 1,724 128.2 128.2 Example 3 141.6 1,780 128.4 128.4 Example 4 145.9 1,833 130.1 130.1 Example 5 153.7 1,932 135.8 135.8 Comparative 126.9 1,595 132.9 132.9 Example 1 Comparative 137.0 1,721 123.7 123.7 Example 2 Comparative 154.4 1,940 126.7 126.7 Example 3 Comparative 102.5 1,288 131.9 131.9 Example 4 Properties of magnetic metal particles containing iron as main component Examples Oxidation and Squareness stability Ignition Comparative (σr/σs) (Δσs) temperature Examples (−) (%) (° C.) Example 2 0.496 4.4 146 Example 3 0.494 3.9 149 Example 4 0.496 3.1 153 Example 5 0.508 4.2 148 Comparative 0.482 6.2 133 Example 1 Comparative 0.490 4.9 141 Example 2 Comparative 0.514 9.5 119 Example 3 Comparative 0.473 11.5 109 Example 4 Properties of magnetic coating film (when Examples oriented in a magnetic field of 5 kOe) and Coercive force Comparative (Hc) Squareness Examples (kA/m) (Oe) (Br/Bm) Example 2 134.6 1,691 0.848 Example 3 140.5 1,765 0.844 Example 4 144.7 1,818 0.841 Example 5 152.0 1,910 0.849 Comparative 124.6 1,566 0.832 Example 1 Comparative 134.3 1,688 0.845 Example 2 Comparative 155.3 1,951 0.870 Example 3 Comparative 99.6 1,251 0.818 Example 4 Properties of magnetic coating film (when Examples oriented in a magnetic field of 5 kOe) and Orientation Comparative property Examples (OR) SFD ΔBm (%) Example 2 3.05 0.488 3.0 Example 3 2.95 0.464 2.8 Example 4 2.88 0.462 2.4 Example 5 2.98 0.450 2.9 Comparative 2.69 0.533 5.8 Example 1 Comparative 2.99 0.502 4.1 Example 2 Comparative 3.55 0.411 6.9 Example 3 Comparative 2.33 0.588 9.9 Example 4 

What is claimed is:
 1. Spindle-shaped magnetic metal particles containing iron as a main component, having an average major axis diameter (L) of 0.05 to 0.15 μm; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of from 150 to less than 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula: S≦−160×L+65; an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.
 2. Spindle-shaped magnetic metal particles containing iron as a main component according to claim 1, which have an Al content of from 5 to 10 atm % based on whole Fe and a rare earth element content of from 1.5 to 5 atm % based on whole Fe.
 3. Spindle-shaped magnetic metal particles containing iron as a main component according to claim 1, which have a size distribution (standard deviation/average major axis diameter) of not more than 0.30 and an aspect ratio of 4:1 to 8:1.
 4. Spindle-shaped magnetic metal particles containing iron as a main component according to claim 1, which are produced by heat-dehydrating spindle-shaped goethite particles to obtain spindle-shaped hematite particles and then heat-reducing the spindle-shaped hematite particles, said spindle-shaped goethite particle comprising a spindle-shaped goethite seed crystal particle containing Co, a goethite layer formed on the surface of the spindle-shaped goethite seed crystal particle, containing Co and Al, and a surface layer form on the goethite layer, comprising cobalt compounds and rare earth compounds, a cobalt content in the spindle-shaped goethite particle being from 0.5 to less than 5 atm % based on whole Fe contained in the spindle-shaped goethite particle; an Al content in the goethite layer being from 5 to 10 atm % based on whole Fe contained in the spindle-shaped goethite particle; an Co content in the surface layer being 20 to 200% based on whole Co contained in the spindle-shaped goethite seed crystal particle containing Co and the goethite layer containing Co, and being from 5 to less than 15 atm % based on whole Fe contained in the spindle-shaped goethite particle; and the rare earth content in the surface layer being 1.5 to 5 atm % based on whole Fe contained in the spindle-shaped goethite particle.
 5. Spindle-shaped magnetic metal particles containing iron as a main component according to claim 1, which are produced by heat-reducing spindle-shaped hematite particles, said spindle-shaped hematite particle comprising a spindle-shaped hematite core particle containing Co, a hematite layer formed on the surface of the spindle-shaped hematite core particle, containing Co and Al, and a surface layer form on the hematite layer, comprising cobalt compounds and rare earth compounds, a cobalt content in the spindle-shaped hematite core particle being from 0.5 to less than 5.atm % based on whole Fe contained in the spindle-shaped hematite particle; an Al content in the hematite layer being from 5 to 10 atm % based on whole Fe contained in the spindle-shaped hematite particle; an Co content in the surface layer being 20 to 200% based on whole Co contained in the spindle-shaped hematite core particle containing Co and the hematite layer containing Co, and being from 5 to less than 15 atm % based on whole Fe contained in the spindle-shaped goethite particle; and the rare earth content in the surface layer being 1.5 to 5 atm % based on whole Fe contained in the spindle-shaped hematite particle.
 6. A process for producing spindle-shaped magnetic metal particles containing iron as a main component, comprising: a first step comprising: aging a water suspension containing a ferrous-containing precipitate produced by reacting a mixed aqueous alkali solution comprising an aqueous alkali carbonate solution and an aqueous alkali hydroxide solution with an aqueous ferrous salt solution, in a non-oxidative atmosphere; conducting an oxidation reaction of the water suspension by passing an oxygen-containing gas therethrough, thereby producing spindle-shaped goethite seed crystal particles; and passing again an oxygen-containing gas through the water suspension containing both the ferrous-containing precipitate and the spindle-shaped goethite seed crystal particles so as to conduct an oxidation reaction thereof, thereby forming a goethite layer on the surface of the seed crystal particles to obtain spindle-shaped goethite particles, upon the production of said seed crystal particles, a Co compound being added in an amount of from 0.5 to less than 5 atm %, calculated as Co, based on whole Fe, to the water suspension containing the ferrous-containing precipitate during the aging thereof but prior to the elapse of 50% of the whole aging time before initiation of the oxidation reaction; the oxidation reaction being conducted while passing the oxygen-containing gas through the water suspension at a superficial velocity of 2.3 to 3.5 cm/s such that 30 to 50% of whole Fe²⁺ is oxidized; an Al compound being added in an amount of 5 to 10 atm %, calculated as Al, based on whole Fe; and the oxidation reaction being successively conducted to obtain spindle-shaped goethite particles; a second step comprising adding an anti-sintering agent containing a rare earth compound in an amount of 1.5 to 5 atm %, calculated as a rare earth element, based on whole Fe and a Co compound in an amount of 20 to 200% based on whole Co contained in the spindle-shaped goethite seed crystal particle containing Co and the goethite layer containing Co, and being from 5 to less than 15 atm % based on whole Fe contained in the spindle-shaped goethite particle; a third step comprising heat-treating the thus treated spindle-shaped goethite particles at a temperature of 650 to 800° C. in a non-reducing atmosphere, thereby obtaining spindle-shaped hematite particles; and a fourth step comprising charging the spindle-shaped hematite particles obtained in the above third step into a reducing apparatus to form a fixed-bed having a height of 3 to 15 cm; heating the fixed-bed of the spindle-shaped hematite particles to a temperature of 400 to 700° C. at a temperature-rising rate of 10 to 80° C./minute in an atmosphere of a reducing gas passed though the reducing apparatus at a superficial velocity of 40 to 150 cm/s, thereby reducing the spindle-shaped hematite particles; and then forming an oxide coating film on the surface of the thus reduced particles, thereby obtaining the magnetic metal particles containing iron as a main component.
 7. A magnetic recording medium comprising: a non-magnetic substrate; and a magnetic recording layer formed on the non-magnetic substrate comprising a binder resin and spindle-shaped magnetic metal particles containing iron as a main component, which have an average major axis diameter (L) of 0.05 to 0.15 μm; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of 150 to 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula: S≦−160×L+65; an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.
 8. A magnetic recording medium comprising: a non-magnetic base film; a non-magnetic undercoat layer formed on said non-magnetic base film; and a magnetic recording layer formed on the non-magnetic substrate comprising a binder resin and spindle-shaped magnetic metal particles containing iron as a main component, which have an average major axis diameter (L) of 0.05 to 0.15 μm; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; a crystallite size of 150 to 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula: S≦−160×L+65; an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C.
 9. Spindle-shaped magnetic metal particles containing iron as a main component, having an average major axis diameter (L) of 0.05 to 0.15 μm; a size distribution (standard deviation/average major axis diameter) of not more than 0.30; an aspect ratio of 4:1 to 8:1; a coercive force of 111.4 to 159.2 kA/m; a Co content of from 5 to less than 15 atm % based on whole Fe; an Al content of from 5 to 10 atm % based on whole Fe; a rare earth element content of from 1.5 to 5 atm % based on whole Fe; a crystallite size of from 150 to less than 170 Å; a ratio of Al to Co from 0.3:1 to less than 2.0:1; a specific surface area (S) represented by the formula: S≦−160×L+65; an oxidation stability (Δσs) of saturation magnetization of not more than 4.5%; and an ignition temperature of not less than 145° C. 